A New Mutation in Rpl10 Associated with X-Linked Syndromic Intellectual Disability in Two Families and Literature Review

AuthID
 P-00Q-ZFY
8
Author(s)
Venancio, M
·
Grote, L
·
Friez, M
·
Chanudet, E
·
Bachelli, C
·
Williams, H
·
Sousa, S
Tipo de Documento
Abstract
Year published
2019
Publicado
in MEDICINE, ISSN: 0025-7974
Volume: 98, Número: 26
Conference
22Nd Annual Meeting of the Portuguese-Society-Of-Human-Genetics (Spgh), Date: NOV 15-17, 2018, Location: Porto, PORTUGAL, Patrocinadores: Portuguese Soc Human Genet
Indexing
Wos®
Publication Identifiers
Wos: WOS:000480733400151
Source Identifiers
ISSN: 0025-7974
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