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Q53158422-08AB033E-0E80-41FB-BE8A-13215E11939D
Q53158422-08AB033E-0E80-41FB-BE8A-13215E11939D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53158422-08AB033E-0E80-41FB-BE8A-13215E11939D
The MECP2 variant c.925C>T (p.Arg309Trp) causes intellectual disability in both males and females without classic features of Rett syndrome.
P2860
Q53158422-08AB033E-0E80-41FB-BE8A-13215E11939D
BestRank
Statement
http://www.wikidata.org/entity/statement/Q53158422-08AB033E-0E80-41FB-BE8A-13215E11939D
rank
NormalRank
type
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wasDerivedFrom
9daaddd6d23187baa4c5b0fb47a3bea8ba583669
P2860
MeCP2: structure and function.