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Q42975330-81C26E71-D50C-4F58-8AB0-EE23EB88AD8A
Q42975330-81C26E71-D50C-4F58-8AB0-EE23EB88AD8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42975330-81C26E71-D50C-4F58-8AB0-EE23EB88AD8A
De novo mutation in ATP6V1B2 impairs lysosome acidification and causes dominant deafness-onychodystrophy syndrome.
P2860
Q42975330-81C26E71-D50C-4F58-8AB0-EE23EB88AD8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42975330-81C26E71-D50C-4F58-8AB0-EE23EB88AD8A
rank
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type
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wasDerivedFrom
cf7b094936379cbfbcdb471d797f3294c1b289b5
P2860
Mutations in SYNGAP1 in autosomal nonsyndromic mental retardation