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Q31111140-F6089647-654A-4D5E-A7AF-B2C0A6B87DC1
Q31111140-F6089647-654A-4D5E-A7AF-B2C0A6B87DC1
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http://www.wikidata.org/entity/statement/Q31111140-F6089647-654A-4D5E-A7AF-B2C0A6B87DC1
Sensory and motor cortex function contributes to symptom severity in spinocerebellar ataxia type 6.
P2860
Q31111140-F6089647-654A-4D5E-A7AF-B2C0A6B87DC1
BestRank
Statement
http://www.wikidata.org/entity/statement/Q31111140-F6089647-654A-4D5E-A7AF-B2C0A6B87DC1
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wasDerivedFrom
e1619dd4ebb09f352f742121b5d48614bbb64189
P2860
Genotype-specific patterns of atrophy progression are more sensitive than clinical decline in SCA1, SCA3 and SCA6.