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Paper Details

Evidence for involvement of GNB1L in autism.
Am J Med Genet B Neuropsychiatr Genet
19
2012
(dup22q11, 1, 22q11, ASDs, GNB1L, GNB1L gene, GNB1L missense variants, TBX1, WD40 repeat domains, autism, autism spectrum disorders, balanced translocation, chromosome 22q11, chromosome-22 breakpoint, cognitive impairment, congenital malformations, del22q11, dup22q11, facial and cardiac malformations, haploinsufficiency for TBX1, immunologic impairments, intron 7, missense variants, neurocognitive abnormalities, schizophrenia, somatic cell hybrids
Author NameAffiliation
Ying-Zhang ChenUniversity of Washington
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Release 1.2