CHCHD2 and Parkinson's disease--authors' reply (Q85360571)

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17 February 2020

title

CHCHD2 and Parkinson's disease--authors' reply (English)

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17 February 2020

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Manabu Funayama

1

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17 February 2020

Nobutaka Hattori

series ordinal

2

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17 February 2020

publication date

1 July 2015

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17 February 2020

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17 February 2020

volume

14

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17 February 2020

issue

7

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17 February 2020

page(s)

682-683

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

17 February 2020

cites work

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7 January 2021

Genome-wide association study identifies common variants at four loci as genetic risk factors for Parkinson's disease

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7 January 2021

Early transcriptional changes linked to naturally occurring Huntington's disease mutations in neural derivatives of human embryonic stem cells.

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7 January 2021

Cyclic adenosine monophosphate response element-binding protein transcriptionally regulates CHCHD2 associated with the molecular pathogenesis of hepatocellular carcinoma

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https://api.crossref.org/works/10.1016%2FS1474-4422%2815%2900097-6

7 January 2021

LRRK2 in Parkinson's disease: genetic and clinical studies from patients

1 reference

https://api.crossref.org/works/10.1016%2FS1474-4422%2815%2900097-6

7 January 2021

The genetics of Parkinson's disease: progress and therapeutic implications

1 reference

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7 January 2021

10.1016/S1474-4422(15)00097-6

Identifiers

DOI

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17 February 2020

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