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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

Crossref DOI link: https://doi.org/10.1016/j.ejmg.2019.103800

Published Print: 2020-04

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Nagy, Dóra

Farkas, Katalin

Armengol, Lluís

Segura, Maria

Esi Zodanu, Gloria Kafui

Csányi, Bernadett

Zimmermann, Alíz

Vámos, Barbara

Széll, Márta
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Text and Data Mining valid from 2020-04-01

Text and Data Mining valid from 2020-04-01
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This article is maintained by: Elsevier

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

Journal Title: European Journal of Medical Genetics

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.ejmg.2019.103800

Content Type: simple-article

Copyright: © 2019 Elsevier Masson SAS. All rights reserved.

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