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Article

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

European journal of medical genetics - 1 Apr 2020

Nagy Dóra, Farkas Katalin, Armengol Lluís, Segura Maria, Esi Zodanu Gloria Kafui, Csányi Bernadett, Zimmermann Alíz, Vámos Barbara, Széll Márta

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Identifiers

PMID: 31678216
DOI: 10.1016/j.ejmg.2019.103800

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Further delineation of the phenotype of PAK3-associated x-linked intellectual disability: Identification of a novel missense mutation and review of literature.PMID 31678216Read ↗

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