Rare Genetic Variation in 135 Families With Family History Suggestive of X-Linked Intellectual Disability

Families with multiple male children with intellectual disability (ID) are usually suspected of having disease due to a X-linked mode of inheritance and genetic studies focus on analysis of segregating variants in X-linked genes. However, the genetic cause of ID remains elusive in approximately 50%...

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Detalles Bibliográficos
Autores principales: Sanchis-Juan, Alba, Bitsara, Christina, Low, Kay Yi, Carss, Keren J., French, Courtney E., Spasic-Boskovic, Olivera, Jarvis, Joanna, Field, Michael, Raymond, F. Lucy, Grozeva, Detelina
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2019
Materias:
Genetics
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609311/
https://www.ncbi.nlm.nih.gov/pubmed/31316545
http://dx.doi.org/10.3389/fgene.2019.00578

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6609311/
https://www.ncbi.nlm.nih.gov/pubmed/31316545
http://dx.doi.org/10.3389/fgene.2019.00578

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