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Q58553606-7DAE7827-08B8-4EA9-A8D4-0389EB8B2693
Q58553606-7DAE7827-08B8-4EA9-A8D4-0389EB8B2693
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58553606-7DAE7827-08B8-4EA9-A8D4-0389EB8B2693
Skeletal disease in a father and daughter with a novel monoallelic WNT1 mutation
P2860
Q58553606-7DAE7827-08B8-4EA9-A8D4-0389EB8B2693
BestRank
Statement
http://www.wikidata.org/entity/statement/Q58553606-7DAE7827-08B8-4EA9-A8D4-0389EB8B2693
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Statement
wasDerivedFrom
c3483ef6a31e71af715eaa0332b4160000d76cad
P2860
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations