A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability

The large majority of cases with intellectual disability are syndromic (i.e. occur with other well-defined clinical phenotypes) and have been studied extensively. Autosomal recessive nonsyndromic intellectual disability is a group of genetically heterogeneous disorders for which a number of potentia...

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Detalles Bibliográficos
Autores principales: Muthusamy, Babylakshmi, Bellad, Anikha, Prasad, Pramada, Bandari, Aravind K., Bhuvanalakshmi, G., Kiragasur, R. M., Girimaji, Satish Chandra, Pandey, Akhilesh
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Psychiatry
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247441/
https://www.ncbi.nlm.nih.gov/pubmed/32499722
http://dx.doi.org/10.3389/fpsyt.2020.00354

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7247441/
https://www.ncbi.nlm.nih.gov/pubmed/32499722
http://dx.doi.org/10.3389/fpsyt.2020.00354

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