Journal
Neurology. Genetics
ISSN: 2376-7839
Titre abrégé: Neurol Genet
Pays: United States
ID NLM: 101671068
Informations de publication
Date de publication:
Apr 2020
Apr 2020
Historique:
received:
16
09
2019
accepted:
17
12
2019
entrez:
27
3
2020
pubmed:
27
3
2020
medline:
27
3
2020
Statut:
epublish
Résumé
To identify the phenotypic, neuroimaging, and genotype-phenotype expression of Using next-generation sequencing, we screened 86 patients with primary familial brain calcification (PFBC) from 60 families with autosomal recessive or absent family history that were negative for mutations in We identified 12 distinct deleterious This large, multicentric study shows that biallelic
Identifiants
pubmed: 32211515
doi: 10.1212/NXG.0000000000000399
pii: NG2019011999
pmc: PMC7073457
doi:
Types de publication
Journal Article
Langues
eng
Pagination
e399Informations de copyright
Copyright © 2020 The Author(s). Published by Wolters Kluwer Health, Inc. on behalf of the American Academy of Neurology.
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