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Q48269069-29FAABBE-EF3C-49D4-8358-69D2BCF2AA3C
Q48269069-29FAABBE-EF3C-49D4-8358-69D2BCF2AA3C
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Statement
http://www.wikidata.org/entity/statement/Q48269069-29FAABBE-EF3C-49D4-8358-69D2BCF2AA3C
A novel gain-of-function mutation in the ITPR1 suppressor domain causes spinocerebellar ataxia with altered Ca2+ signal patterns.
P2860
Q48269069-29FAABBE-EF3C-49D4-8358-69D2BCF2AA3C
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48269069-29FAABBE-EF3C-49D4-8358-69D2BCF2AA3C
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type
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wasDerivedFrom
8a33f0687f3f5bf3916549d4fbdf33d21247bdaa
P2860
Role of inositol 1,4,5-trisphosphate receptors in pathogenesis of Huntington's disease and spinocerebellar ataxias