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Q36369911-6157672A-D6DE-4B77-993F-6B2C85992D3F
Q36369911-6157672A-D6DE-4B77-993F-6B2C85992D3F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36369911-6157672A-D6DE-4B77-993F-6B2C85992D3F
Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.
P2860
Q36369911-6157672A-D6DE-4B77-993F-6B2C85992D3F
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36369911-6157672A-D6DE-4B77-993F-6B2C85992D3F
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4f40309b8a65a05382bdf8dabe3c23de691a1d95
P2860
Hereditary ataxias: overview.