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Q34144191-A01F220B-2F01-4516-9F02-C6AAE4D59D70
Q34144191-A01F220B-2F01-4516-9F02-C6AAE4D59D70
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Statement
http://www.wikidata.org/entity/statement/Q34144191-A01F220B-2F01-4516-9F02-C6AAE4D59D70
A mutation in the rett syndrome gene, MECP2, causes X-linked mental retardation and progressive spasticity in males
P2860
Q34144191-A01F220B-2F01-4516-9F02-C6AAE4D59D70
BestRank
Statement
http://www.wikidata.org/entity/statement/Q34144191-A01F220B-2F01-4516-9F02-C6AAE4D59D70
rank
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type
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Statement
wasDerivedFrom
24a07e2e166ad5e9d747d1a8ba8cb8ae86f896dd
P2860
Rett syndrome and beyond: recurrent spontaneous and familial MECP2 mutations at CpG hotspots