mental retardation, X-linked 59

Genetics

• associated with defects in AP1S2

Clinical manifestations

• mild-to-profound mental retardation
• hypotonia early in life
• delay in walking

More general terms

• X-linked mental retardation

Database

• OMIM: https://mirror.omim.org/entry/300630
• Entrez gene: http://www.ncbi.nlm.nih.gov/sites/entrez?db=gene&cmd=Retrieve&dopt=Graphics&list_uids=4422