(Q42931762)

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

title

Reply: Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis (English)

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

amyotrophic lateral sclerosis

20 February 2020

main subject

0 references

author

Emmanuelle C Genin

4

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Valérie Serre

9

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

David Moore

10

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Francoise Lespinasse

16

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

author name string

Sylvie Bannwarth

1

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Samira Ait-El-Mkadem

2

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Annabelle Chaussenot

3

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Sandra Lacas-Gervais

5

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Konstantina Fragaki

6

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Laetitia Berg-Alonso

7

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Yusuke Kageyama

8

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Annie Verschueren

11

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Cécile Rouzier

12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Isabelle Le Ber

13

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Gaëlle Augé

14

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Charlotte Cochaud

15

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Karine N'Guyen

17

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Anne de Septenville

18

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Alexis Brice

19

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Patrick Yu-Wai-Man

20

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Hiromi Sesaki

21

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

Jean Pouget

22

1 reference

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20 February 2020

Véronique Paquis-Flucklinger

23

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

language of work or name

English

0 references

publication date

26 September 2014

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

volume

137

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

issue

Pt 12

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

page(s)

e312

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

A mitochondrial origin for frontotemporal dementia and amyotrophic lateral sclerosis through CHCHD10 involvement

20 February 2020

cites work

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4809975

Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

27 May 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4809975

Screening of CHCHD10 in a French cohort confirms the involvement of this gene in frontotemporal dementia with amyotrophic lateral sclerosis patients.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4809975

Two novel mutations in conserved codons indicate that CHCHD10 is a gene associated with motor neuron disease.

16 August 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4809975

16 August 2018

Identifiers

DOI

10.1093/BRAIN/AWU267

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json

20 February 2020

1 reference

https://www.ebi.ac.uk/europepmc/webservices/rest/search?query=EXT_ID:25261971%20AND%20SRC:MED&resulttype=core&format=json