Arthrogryposis multiplex congenita with polymicrogyria and infantile encephalopathy caused by a novel
Epilepsy
Paediatric neurological disorders
Journal
Human genome variation
ISSN: 2054-345X
Titre abrégé: Hum Genome Var
Pays: England
ID NLM: 101652445
Informations de publication
Date de publication:
2020
2020
Historique:
received:
30
04
2020
revised:
11
08
2020
accepted:
13
08
2020
entrez:
16
10
2020
pubmed:
17
10
2020
medline:
17
10
2020
Statut:
epublish
Résumé
Variants of
Identifiants
pubmed: 33062288
doi: 10.1038/s41439-020-00116-8
pii: 116
pmc: PMC7519642
doi:
Types de publication
Journal Article
Langues
eng
Pagination
29Informations de copyright
© The Author(s) 2020.
Déclaration de conflit d'intérêts
Conflict of interestThe authors declare that they have no conflict of interest.
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