A Novel LINS1 Truncating Mutation in Autosomal Recessive Nonsyndromic Intellectual Disability

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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Bibliographic Details
Main Authors: Babylakshmi Muthusamy, Anikha Bellad, Pramada Prasad, Aravind K. Bandari, G. Bhuvanalakshmi, R. M. Kiragasur, Satish Chandra Girimaji, Akhilesh Pandey
Format: Article
Language:English
Published: Frontiers Media S.A. 2020-05-01
Series:Frontiers in Psychiatry
Subjects:
autosomal recessive
truncating mutation
WNT signalling
Embryogenesis
genetic disorders
Online Access:https://www.frontiersin.org/article/10.3389/fpsyt.2020.00354/full

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https://www.frontiersin.org/article/10.3389/fpsyt.2020.00354/full

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