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Q38915057-0FD2B059-ECD9-42A4-A856-8E4E671BB69E
Q38915057-0FD2B059-ECD9-42A4-A856-8E4E671BB69E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38915057-0FD2B059-ECD9-42A4-A856-8E4E671BB69E
Cerebellar ataxias: β-III spectrin's interactions suggest common pathogenic pathways.
P2860
Q38915057-0FD2B059-ECD9-42A4-A856-8E4E671BB69E
BestRank
Statement
http://www.wikidata.org/entity/statement/Q38915057-0FD2B059-ECD9-42A4-A856-8E4E671BB69E
rank
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type
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wasDerivedFrom
812a615ddee8619a820388d45b0bad1a384702dd
P2860
Mutations in the mitochondrial protease gene AFG3L2 cause dominant hereditary ataxia SCA28.