Genomics

Dataset Information

0

EGAS00001000775-sc-20181010 - samples


ABSTRACT: DDD DATAFREEZE 2017-12-15: 13,462 trios and probands only - phenotypic and family descriptions

PROVIDER: EGAD00001004388 | EGA |

REPOSITORIES: EGA

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Publications


Here we report inherited dysregulation of protein phosphatase activity as a cause of intellectual disability (ID). De novo missense mutations in 2 subunits of serine/threonine (Ser/Thr) protein phosphatase 2A (PP2A) were identified in 16 individuals with mild to severe ID, long-lasting hypotonia, epileptic susceptibility, frontal bossing, mild hypertelorism, and downslanting palpebral fissures. PP2A comprises catalytic (C), scaffolding (A), and regulatory (B) subunits that determine subcellular  ...[more]

Publication: 1/2

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