Spastic paraplegia due to recessive or dominant mutations in
Journal
Neurology. Genetics
ISSN: 2376-7839
Titre abrégé: Neurol Genet
Pays: United States
ID NLM: 101671068
Informations de publication
Date de publication:
Dec 2019
Dec 2019
Historique:
received:
07
06
2019
accepted:
05
09
2019
entrez:
12
2
2020
pubmed:
12
2
2020
medline:
12
2
2020
Statut:
epublish
Résumé
The aim of this study was to evaluate whether mutations in Whole-exome sequencing was performed in a large cohort of 200 familial ALS and 60 sporadic ALS after a systematic screening for Here, we report the identification of Inheritance of
Identifiants
pubmed: 32042907
doi: 10.1212/NXG.0000000000000374
pii: NG2019011064
pmc: PMC6927358
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e374Informations de copyright
Copyright © 2019 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
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