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1
Q41937036-5C9A0DD1-2F68-4B3F-91BE-E57D1101C62E
Q41937036-5C9A0DD1-2F68-4B3F-91BE-E57D1101C62E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41937036-5C9A0DD1-2F68-4B3F-91BE-E57D1101C62E
Acquired microcephaly, regression of milestones, mitochondrial dysfunction, and episodic rigidity in a 46,XY male with a de novo MECP2 gene mutation.
P2860
Q41937036-5C9A0DD1-2F68-4B3F-91BE-E57D1101C62E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q41937036-5C9A0DD1-2F68-4B3F-91BE-E57D1101C62E
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
b54b9930c1f208ee9495cda7fd4f78bc4aa61cbc
P2860
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2