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1
Q48959079-A693F668-34E7-438C-9DE1-64E4AE068A67
Q48959079-A693F668-34E7-438C-9DE1-64E4AE068A67
BestRank
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http://www.wikidata.org/entity/statement/Q48959079-A693F668-34E7-438C-9DE1-64E4AE068A67
Diagnostic utility of whole exome sequencing in patients showing cerebellar and/or vermis atrophy in childhood.
P2860
Q48959079-A693F668-34E7-438C-9DE1-64E4AE068A67
BestRank
Statement
http://www.wikidata.org/entity/statement/Q48959079-A693F668-34E7-438C-9DE1-64E4AE068A67
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wasDerivedFrom
7613c9f40ee3842c768a4ca404c29e37f3d278a1
P2860
Missense mutations in ITPR1 cause autosomal dominant congenital nonprogressive spinocerebellar ataxia.