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Q37058036-B2F64326-94B3-4DA2-9E27-DEE1F6F64A30
Q37058036-B2F64326-94B3-4DA2-9E27-DEE1F6F64A30
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058036-B2F64326-94B3-4DA2-9E27-DEE1F6F64A30
Pathogenic CWF19L1 variants as a novel cause of autosomal recessive cerebellar ataxia and atrophy.
P2860
Q37058036-B2F64326-94B3-4DA2-9E27-DEE1F6F64A30
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37058036-B2F64326-94B3-4DA2-9E27-DEE1F6F64A30
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Statement
wasDerivedFrom
4af03d72e2106596b972b38d5392ea00197e7667
P2860
A novel syndrome of Klippel-Feil anomaly, myopathy, and characteristic facies is linked to a null mutation in MYO18B.