WDR13: A Novel Gene Implicated in Non-Syndromic Intellectual Disability

Investigating novel genetic variants involved in intellectual disability (ID) development is essential. X-linked intellectual disability (XLID) accounts for over 10% of all cases of ID in males. XLID genes are involved in many cellular pathways and processes. Some of them are not specific to the dev...

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Detalles Bibliográficos
Autores principales: Rzońca-Niewczas, Sylwia, Wierzba, Jolanta, Kaczorowska, Ewa, Poryszewska, Milena, Kosińska, Joanna, Stawiński, Piotr, Płoski, Rafał, Bal, Jerzy
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2021
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701106/
https://www.ncbi.nlm.nih.gov/pubmed/34946860
http://dx.doi.org/10.3390/genes12121911

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8701106/
https://www.ncbi.nlm.nih.gov/pubmed/34946860
http://dx.doi.org/10.3390/genes12121911

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