CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study (Q28114901)

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29 February 2020

title

CHCHD2 mutations in autosomal dominant late-onset Parkinson's disease: a genome-wide linkage and sequencing study (English)

2 references

3 January 2017

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29 February 2020

1 reference

Coiled-coil-helix-coiled-coil-helix domain containing 2

1 reference

GOA release 2020-03-11

author

Manabu Funayama

1

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29 February 2020

Kaoru Mogushi

16

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29 February 2020

Kinji Ohno

23

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29 February 2020

author name string

Kenji Ohe

2

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3 January 2017

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29 February 2020

Taku Amo

3

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3 January 2017

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29 February 2020

Norihiko Furuya

4

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3 January 2017

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29 February 2020

Junji Yamaguchi

5

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3 January 2017

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29 February 2020

Shinji Saiki

6

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3 January 2017

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29 February 2020

Yuanzhe Li

7

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3 January 2017

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29 February 2020

Kotaro Ogaki

8

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3 January 2017

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29 February 2020

Maya Ando

9

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3 January 2017

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29 February 2020

Hiroyo Yoshino

10

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3 January 2017

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29 February 2020

Hiroyuki Tomiyama

11

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3 January 2017

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29 February 2020

Kenya Nishioka

12

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3 January 2017

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29 February 2020

Kazuko Hasegawa

13

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3 January 2017

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29 February 2020

Hidemoto Saiki

14

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3 January 2017

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29 February 2020

Wataru Satake

15

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3 January 2017

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29 February 2020

Ryogen Sasaki

17

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3 January 2017

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29 February 2020

Yasumasa Kokubo

18

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3 January 2017

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29 February 2020

Shigeki Kuzuhara

19

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3 January 2017

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29 February 2020

Tatsushi Toda

20

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3 January 2017

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29 February 2020

Yasuo Uchiyama

22

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3 January 2017

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29 February 2020

Yoshikuni Mizuno

21

1 reference

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29 February 2020

Nobutaka Hattori

24

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29 February 2020

publication date

4 February 2015

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29 February 2020

2 references

3 January 2017

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29 February 2020

volume

14

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29 February 2020

page(s)

274-282

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29 February 2020

issue

3

2 references

3 January 2017

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Familial aggregation of Parkinson's disease in a multiethnic community-based case-control study

29 February 2020

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Mutations in the GIGYF2 (TNRC15) gene at the PARK11 locus in familial Parkinson disease

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hnRNP H enhances skipping of a nonfunctional exon P3A in CHRNA1 and a mutation disrupting its binding causes congenital myasthenic syndrome

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Oxygen-dependent expression of cytochrome c oxidase subunit 4-2 gene expression is mediated by transcription factors RBPJ, CXXC5 and CHCHD2

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Identifiers

DOI

2 references

Consolidated OpenCitations Corpus – April 2017

5474

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29 February 2020

5474

1 reference

Consolidated OpenCitations Corpus – April 2017

Consolidated OpenCitations Corpus – April 2017

2 references

5474