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

J. O. Johnson; S. M. Glynn; Gibbs J. Raphael; M. A. Nalls; Mario Sabatelli; G. Restagno; V. E. Drory; A. Chio; E. Rogaeva; B. J. Traynor

doi:10.1093/brain/awu265

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

J. O. Johnson
, S. M. Glynn
, Gibbs J. Raphael
, M. A. Nalls
, Mario Sabatelli
, G. Restagno
, V. E. Drory
, A. Chio
, E. Rogaeva
, B. J. Traynor^*

^*Autore corrispondente per questo lavoro

Risultato della ricerca: Contributo in rivista › Articolo

86 Citazioni (Scopus)

Abstract

n/a

Lingua originale	Inglese
pagine (da-a)	e311-e311
Rivista	Brain
Volume	137
Numero di pubblicazione	12
DOI	https://doi.org/10.1093/brain/awu265
Stato di pubblicazione	Pubblicato - 2014

All Science Journal Classification (ASJC) codes

Neurologia (clinica)

Keywords

Amyotrophic Lateral Sclerosis
DNA
Female
Frontotemporal Dementia
Humans
Male
Mitochondria
Mitochondrial
Mitochondrial Diseases
Mitochondrial Proteins

Accesso al documento

10.1093/brain/awu265

Altri file e collegamenti

Cita questo

@article{d76299bbd0ff49c6995752ccd915d9b4,

title = "Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis",

abstract = "n/a",

keywords = "Amyotrophic Lateral Sclerosis, DNA, Female, Frontotemporal Dementia, Humans, Male, Mitochondria, Mitochondrial, Mitochondrial Diseases, Mitochondrial Proteins, Amyotrophic Lateral Sclerosis, DNA, Female, Frontotemporal Dementia, Humans, Male, Mitochondria, Mitochondrial, Mitochondrial Diseases, Mitochondrial Proteins",

author = "Johnson, \{J. O.\} and Glynn, \{S. M.\} and Raphael, \{Gibbs J.\} and Nalls, \{M. A.\} and Mario Sabatelli and G. Restagno and Drory, \{V. E.\} and A. Chio and E. Rogaeva and Traynor, \{B. J.\}",

year = "2014",

doi = "10.1093/brain/awu265",

language = "English",

volume = "137",

pages = "e311--e311",

journal = "Brain",

issn = "0006-8950",

publisher = "Oxford University Press",

number = "12",

}

TY - JOUR

T1 - Mutations in the CHCHD10 gene are a common cause of familial amyotrophic lateral sclerosis

AU - Johnson, J. O.

AU - Glynn, S. M.

AU - Raphael, Gibbs J.

AU - Nalls, M. A.

AU - Sabatelli, Mario

AU - Restagno, G.

AU - Drory, V. E.

AU - Chio, A.

AU - Rogaeva, E.

AU - Traynor, B. J.

PY - 2014

Y1 - 2014

N2 - n/a

AB - n/a

KW - Amyotrophic Lateral Sclerosis

KW - DNA

KW - Female

KW - Frontotemporal Dementia

KW - Humans

KW - Male

KW - Mitochondria

KW - Mitochondrial

KW - Mitochondrial Diseases

KW - Mitochondrial Proteins

KW - Amyotrophic Lateral Sclerosis

KW - DNA

KW - Female

KW - Frontotemporal Dementia

KW - Humans

KW - Male

KW - Mitochondria

KW - Mitochondrial

KW - Mitochondrial Diseases

KW - Mitochondrial Proteins

UR - https://publicatt.unicatt.it/handle/10807/140222

UR - https://www.scopus.com/inward/citedby.uri?partnerID=HzOxMe3b&scp=84920873336&origin=inward

UR - https://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=84920873336&origin=inward

U2 - 10.1093/brain/awu265

DO - 10.1093/brain/awu265

M3 - Article

SN - 0006-8950

VL - 137

SP - e311-e311

JO - Brain

JF - Brain

IS - 12

ER -

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

Abstract

All Science Journal Classification (ASJC) codes

Keywords

Accesso al documento

Altri file e collegamenti

Fingerprint

Cita questo