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Q24299351-33494042-ED80-44AC-BBBD-92F6B58834D3
Q24299351-33494042-ED80-44AC-BBBD-92F6B58834D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299351-33494042-ED80-44AC-BBBD-92F6B58834D3
Frequency of KCNC3 DNA variants as causes of spinocerebellar ataxia 13 (SCA13)
P2860
Q24299351-33494042-ED80-44AC-BBBD-92F6B58834D3
BestRank
Statement
http://www.wikidata.org/entity/statement/Q24299351-33494042-ED80-44AC-BBBD-92F6B58834D3
rank
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wasDerivedFrom
a3015d793f5c723e1a065099ac0cc45b33e7476c
P2860
Spinocerebellar ataxia type 28: a novel autosomal dominant cerebellar ataxia characterized by slow progression and ophthalmoparesis.