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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Detalhes bibliográficos
Publicado no:Front Psychiatry
Main Authors: Muthusamy, Babylakshmi, Bellad, Anikha, Prasad, Pramada, Bandari, Aravind K., Bhuvanalakshmi, G., Kiragasur, R. M., Girimaji, Satish Chandra, Pandey, Akhilesh
Formato: Artigo
Idioma:Inglês
Publicado em: Frontiers Media S.A. 2020
Assuntos:
Psychiatry
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC7247441/
https://ncbi.nlm.nih.gov/pubmed/32499722
https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3389/fpsyt.2020.00354
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