Exons deletion of CNKSR2 gene identified in X-linked syndromic intellectual disability

BACKGROUND: The Houge type of X-linked syndromic mental retardation is an X-linked intellectual disability (XLID) recently recorded in the Online Mendelian Inheritance in Man (OMIM) and only 8 cases have been reported in literature thus far. CASE PRESENTATION: We present two brothers with intractabl...

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Detalles Bibliográficos
Autores principales: Daoqi, Mei, Guohong, Chen, Yuan, Wang, Zhixiao, Yang, Kaili, Xu, Shiyue, Mei
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2020
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119275/
https://www.ncbi.nlm.nih.gov/pubmed/32245427
http://dx.doi.org/10.1186/s12881-020-01004-2

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7119275/
https://www.ncbi.nlm.nih.gov/pubmed/32245427
http://dx.doi.org/10.1186/s12881-020-01004-2

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