Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature

Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature

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Bibliographic Details
Published in:European journal of medical genetics Vol. 63; no. 4; p. 103800
Main Authors: Nagy, Dóra, Farkas, Katalin, Armengol, Lluís, Segura, Maria, Esi Zodanu, Gloria Kafui, Csányi, Bernadett, Zimmermann, Alíz, Vámos, Barbara, Széll, Márta
Format: Journal Article
Language:English
Published: Netherlands Elsevier Masson SAS 01-04-2020
Online Access:Get full text
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Description
Bibliography:SourceType-Scholarly Journals-1
ObjectType-Correspondence-1
content type line 23
ObjectType-Report-3
ObjectType-Review-2
ObjectType-Case Study-4
ISSN:1769-7212
1878-0849
DOI:10.1016/j.ejmg.2019.103800