The Role of a Novel TRMT1 Gene Mutation and Rare GRM1 Gene Defect in Intellectual Disability in Two Azeri Families

Cognitive impairment or intellectual disability (ID) is a widespread neurodevelopmental disorder characterized by low IQ (below 70). ID is genetically heterogeneous and is estimated to affect 1–3% of the world’s population. In affected children from consanguineous families, autosomal recessive inher...

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Detalles Bibliográficos
Autores principales: Davarniya, Behzad, Hu, Hao, Kahrizi, Kimia, Musante, Luciana, Fattahi, Zohreh, Hosseini, Masoumeh, Maqsoud, Fariba, Farajollahi, Reza, Wienker, Thomas F., Ropers, H. Hilger, Najmabadi, Hossein
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2015
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550366/
https://www.ncbi.nlm.nih.gov/pubmed/26308914
http://dx.doi.org/10.1371/journal.pone.0129631

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4550366/
https://www.ncbi.nlm.nih.gov/pubmed/26308914
http://dx.doi.org/10.1371/journal.pone.0129631

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