SOD1, ANG, VAPB, TARDBP, and FUS mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

2010293 citationsJournal Articlegreen Open Access

Authors

Stéphanie Millecamps · Centre National de la Recherche Scientifique

François Salachas · Sorbonne Université

C. Cazeneuve · Sorbonne Université

Gordon Gilbert · Pitié-Salpêtrière Hospital

Bernard Bricka · Assistance Publique – Hôpitaux de Paris

A. Camuzat · Institut du Cerveau

Léna Guillot‐Noël

Abstract

This study identifies new genetic associations with ALS and provides phenotype-genotype correlations with both previously reported and novel mutations.

Topics & Keywords

Amyotrophic Lateral Sclerosis Research Neurogenetic and Muscular Disorders Research

Publication Details

Published in: Journal of Medical Genetics

Volume 47, Issue 8, pp. 554-560

DOI: 10.1136/jmg.2010.077180

Field-Weighted Citation Impact: 17.74

Command Palette

<i>SOD1</i>, <i>ANG</i>, <i>VAPB</i>, <i>TARDBP</i>, and <i>FUS</i> mutations in familial amyotrophic lateral sclerosis: genotype–phenotype correlations

Authors

Abstract

Topics & Keywords

Publication Details