De Novo Truncating Mutations in Wasf1 Cause Intellectual Disability with Seizures

AuthID
 P-00P-08R
19
Author(s)
Carss, KJ
·
Keren, B
·
Kurian, MA
·
Marey, I
·
Charles, P
·
Mendonca, C
·
Pfundt, R
·
Sanchis Juan, A
·
van Bokhoven, H
·
van Essen, A
·
van Ravenswaaij Arts, C
·
Dyack, S
·
2
Group Author(s)
NIHR BioResource; Care4Rare Canada Consortium
Tipo de Documento
Article
Year published
2018
Publicado
in AMERICAN JOURNAL OF HUMAN GENETICS, ISSN: 0002-9297
Volume: 103, Número: 1, Páginas: 144-153 (10)
Indexing
Wos®
Google Scholar®
Publication Identifiers
Wos: WOS:000438168800013
Source Identifiers
ISSN: 0002-9297
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