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De Novo Truncating Mutations in Wasf1 Cause Intellectual Disability with Seizures
AuthID
P-00P-08R
19
Author(s)
Ito, Y
·
Carss, KJ
·
Duarte, ST
·
Hartley, T
·
Keren, B
·
Kurian, MA
·
Marey, I
·
Charles, P
·
Mendonca, C
·
Nava, C
·
Pfundt, R
·
Sanchis Juan, A
·
van Bokhoven, H
·
van Essen, A
·
van Ravenswaaij Arts, C
·
Boycott, KM
·
Kernohan, KD
·
Dyack, S
·
Raymond, FL
2
Group Author(s)
NIHR BioResource; Care4Rare Canada Consortium
Document Type
Article
Year published
2018
Published
in
AMERICAN JOURNAL OF HUMAN GENETICS,
ISSN: 0002-9297
Volume: 103, Issue: 1, Pages: 144-153 (10)
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Wos
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Metadata
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Publication Identifiers
DOI
:
10.1016/j.ajhg.2018.06.001
Wos
: WOS:000438168800013
Source Identifiers
ISSN
: 0002-9297
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