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Q36369911-52C955AC-B41B-44B9-BD1B-0FE1A0591D88
Q36369911-52C955AC-B41B-44B9-BD1B-0FE1A0591D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36369911-52C955AC-B41B-44B9-BD1B-0FE1A0591D88
Disruptive SCYL1 Mutations Underlie a Syndrome Characterized by Recurrent Episodes of Liver Failure, Peripheral Neuropathy, Cerebellar Atrophy, and Ataxia.
P2860
Q36369911-52C955AC-B41B-44B9-BD1B-0FE1A0591D88
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36369911-52C955AC-B41B-44B9-BD1B-0FE1A0591D88
rank
NormalRank
type
BestRank
Statement
wasDerivedFrom
4f40309b8a65a05382bdf8dabe3c23de691a1d95
P2860
Exome sequencing in undiagnosed inherited and sporadic ataxias