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Q36983068-7B45AD49-A1D8-4413-B3FE-9AFFE714BF09
Q36983068-7B45AD49-A1D8-4413-B3FE-9AFFE714BF09
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Statement
http://www.wikidata.org/entity/statement/Q36983068-7B45AD49-A1D8-4413-B3FE-9AFFE714BF09
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
P2860
Q36983068-7B45AD49-A1D8-4413-B3FE-9AFFE714BF09
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-7B45AD49-A1D8-4413-B3FE-9AFFE714BF09
rank
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Statement
wasDerivedFrom
64c9bf184ba26fd67f14bdd1d275a3dd0f9b6413
P2860
Mutations in PTF1A cause pancreatic and cerebellar agenesis