Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. (Q53532682)

15 May 2018

title

Analysis of PARK genes in a Korean cohort of early-onset Parkinson disease. (English)

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15 May 2018

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10

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Yun J Kim

Yun Joong Kim

21

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Phil Hyu Lee

11

Phil Hyu Lee

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15 May 2018

1

Jung Mi Choi

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15 May 2018

Myoung Soo Woo

2

Myoung Soo Woo

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Hyeo-Il Ma

3

Hyeo-Il Ma

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Suk Yun Kang

4

Suk Yun Kang

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Young-Hee Sung

5

Young-Hee Sung

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Seok Woo Yong

6

Seok Woo Yong

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Sun Ju Chung

7

Sun Ju Chung

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Joong-Seok Kim

8

Joong-Seok Kim

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Hae-won Shin

9

Hae-won Shin

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Jong Sam Baik

12

Jong Sam Baik

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Sang-Jin Kim

13

Sang-Jin Kim

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Mee Young Park

14

Mee Young Park

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15 May 2018

Young H. Sohn

15

Young Ho Sohn

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Jin-Ho Kim

16

Jin-Ho Kim

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15 May 2018

Myung Sik Lee

18

Myung Sik Lee

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Myoung Chong Lee

19

Myoung Chong Lee

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15 May 2018

Dong-Hyun Kim

20

Dong-Hyun Kim

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15 May 2018

author name string

Jae Woo Kim

17

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15 May 2018

publication date

15 August 2008

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15 May 2018

published in

Neurogenetics

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15 May 2018

volume

9

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15 May 2018

page(s)

263-269

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15 May 2018

issue

4

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15 May 2018

https://scigraph.springernature.com/pub.10.1007/s10048-008-0138-0

exact match

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cites work

Improved accuracy of clinical diagnosis of Lewy body Parkinson's disease

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Crossref

https://api.crossref.org/works/10.1007%2FS10048-008-0138-0

The Ala53Thr mutation in the α-synuclein gene in a Korean family with Parkinson disease

21 January 2018

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12 December 2020

Genetic testing in spinocerebellar ataxia in Taiwan: expansions of trinucleotide repeats in SCA8 and SCA17 are associated with typical Parkinson's disease

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12 December 2020

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes.

1 reference

12 December 2020

Multiplex ligation-dependent probe amplification assay for simultaneous detection of Parkinson's disease gene rearrangements

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12 December 2020

PINK1, Parkin, and DJ-1 mutations in Italian patients with early-onset parkinsonism.

1 reference

12 December 2020

A common missense variant in the LRRK2 gene, Gly2385Arg, associated with Parkinson's disease risk in Taiwan

1 reference

12 December 2020

The G2019S LRRK2 mutation is rare in Korean patients with Parkinson's disease.

1 reference

12 December 2020

The LRRK2 Gly2385Arg variant is associated with Parkinson's disease: genetic and functional evidence.

1 reference

12 December 2020

PINK1 mutations are associated with sporadic early-onset parkinsonism

1 reference

12 December 2020

1 reference

12 December 2020

Distribution, type, and origin of Parkin mutations: review and case studies

1 reference

12 December 2020

Detection of Parkin (PARK2) and DJ1 (PARK7) mutations in early-onset Parkinson disease: Parkin mutation frequency depends on ethnic origin of patients.

1 reference

12 December 2020

Rapid and reliable detection of exon rearrangements in various movement disorders genes by multiplex ligation-dependent probe amplification

1 reference

12 December 2020

When Is Ataxia Not Ataxia?

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12 December 2020

Genetic testing in Parkinson disease: promises and pitfalls

1 reference

12 December 2020

The importance of gene dosage studies: mutational analysis of the parkin gene in early-onset parkinsonism

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12 December 2020

Clinical Features and Gene Analysis in Korean Patients With Early-Onset Parkinson Disease

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12 December 2020

Heterozygousparkinpoint mutations are as common in control subjects as in Parkinson's patients

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12 December 2020

Parkinson disease, 10 years after its genetic revolution: multiple clues to a complex disorder

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12 December 2020

Association between early-onset Parkinson's disease and mutations in the parkin gene

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12 December 2020

Clinical Spectrum of Homozygous and Heterozygous PINK1 Mutations in a Large German Family With Parkinson Disease

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12 December 2020

Early-onset parkinsonism associated with PINK1 mutations: frequency, genotypes, and phenotypes

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12 December 2020

Leucine-rich repeat kinase 2 G2385R variant is a risk factor for Parkinson disease in Asian population.

1 reference

12 December 2020

PINK1 mutations in sporadic early-onset Parkinson's disease

1 reference

12 December 2020

The G2019S LRRK2 mutation is uncommon in an Asian cohort of Parkinson's disease patients.

1 reference

12 December 2020

Clinicogenetic study of PINK1 mutations in autosomal recessive early-onset parkinsonism

1 reference

12 December 2020

An LRRK2 mutation as a cause for the parkinsonism in the original PARK8 family.

1 reference

12 December 2020

Analysis of Parkinson disease patients from Portugal for mutations in SNCA, PRKN, PINK1 and LRRK2

1 reference

12 December 2020

10.1007/S10048-008-0138-0

Identifiers

DOI

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15 May 2018

PubMed ID

18704525

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15 May 2018