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Q44455973-E238F7BB-62D1-4B6D-9647-477ECB3FE2FB
Q44455973-E238F7BB-62D1-4B6D-9647-477ECB3FE2FB
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Statement
http://www.wikidata.org/entity/statement/Q44455973-E238F7BB-62D1-4B6D-9647-477ECB3FE2FB
A novel missense mutation in AFG3L2 associated with late onset and slow progression of spinocerebellar ataxia type 28.
P2860
Q44455973-E238F7BB-62D1-4B6D-9647-477ECB3FE2FB
BestRank
Statement
http://www.wikidata.org/entity/statement/Q44455973-E238F7BB-62D1-4B6D-9647-477ECB3FE2FB
rank
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wasDerivedFrom
ff6c128c868f13a10cefd95c132ac5ed1cdd0532
P2860
SCA28, a novel form of autosomal dominant cerebellar ataxia on chromosome 18p11.22-q11.2.