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Q21202871-0BDF066A-BA48-492C-AE7C-DE3CBC2A6E99
Q21202871-0BDF066A-BA48-492C-AE7C-DE3CBC2A6E99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21202871-0BDF066A-BA48-492C-AE7C-DE3CBC2A6E99
X-linked disorders with cerebellar dysgenesis
P2860
Q21202871-0BDF066A-BA48-492C-AE7C-DE3CBC2A6E99
BestRank
Statement
http://www.wikidata.org/entity/statement/Q21202871-0BDF066A-BA48-492C-AE7C-DE3CBC2A6E99
rank
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type
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Statement
wasDerivedFrom
68bd68f1cf80eff69693d34058ac88064095a932
P2860
Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2