Developmental and genetic diseases
Xp22
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Mental retardation, X-linked 59
*Gene map locus Xp22
MRX59
[Clinical features: mild to severe mental retardation; hypotonia in childhood]
[Inheritance: X-linked]
Mutations in the Gene Encoding the Sigma 2 Subunit of the Adaptor Protein 1 Complex, AP1S2, Cause X-Linked Mental Retardation
Mutations in the AP1S2 gene encoding the sigma 2 subunit of the adaptor protein 1 complex are associated with syndromic X-linked mental retardation with hydrocephalus and calcifications in basal ganglia
American Journal of Human Genetics
Journal of Medical Genetics
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Edited by Aldo Campana, February 8, 2010