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Q37058036-2DF18082-0CAA-4F0B-80CE-7B8E95900F20
Q37058036-2DF18082-0CAA-4F0B-80CE-7B8E95900F20
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Statement
http://www.wikidata.org/entity/statement/Q37058036-2DF18082-0CAA-4F0B-80CE-7B8E95900F20
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy.
P2860
Q37058036-2DF18082-0CAA-4F0B-80CE-7B8E95900F20
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058036-2DF18082-0CAA-4F0B-80CE-7B8E95900F20
rank
NormalRank
type
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Statement
wasDerivedFrom
bafe4ecd5df6e281d4aac7a7b06aa01e502fe824
P2860
dbNSFP v2.0: a database of human non-synonymous SNVs and their functional predictions and annotations.