GPR126 : A novel candidate gene implicated in autosomal recessive intellectual disability
Author:
Affiliation:
1. Genetics Research CenterUniversity of Social Welfare and Rehabilitation Sciences Tehran Iran
2. Department Human Molecular GeneticsMax‐Planck‐Institute for Molecular Genetics Berlin Germany
Publisher
Wiley
Subject
Genetics (clinical),Genetics
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1002/ajmg.a.40531
Reference42 articles.
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2. Biallelic variants in LINGO1 are associated with autosomal recessive intellectual disability, microcephaly, speech and motor delay;Ansar M.;Genetics in Medicine,2017
3. The adhesion GPCRs: A unique family of G protein‐coupled receptors with important roles in both central and peripheral tissues;Bjarnadóttir T. K.;Cellular and Molecular Life Sciences,2007
4. LAMA2‐related congenital muscular dystrophy complicated by West syndrome;Camacho A.;European Journal of Paediatric Neurology,2015
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