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Q36983068-A05978A4-E262-48E6-8A79-3147B68C4B75
Q36983068-A05978A4-E262-48E6-8A79-3147B68C4B75
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Statement
http://www.wikidata.org/entity/statement/Q36983068-A05978A4-E262-48E6-8A79-3147B68C4B75
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
P2860
Q36983068-A05978A4-E262-48E6-8A79-3147B68C4B75
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-A05978A4-E262-48E6-8A79-3147B68C4B75
rank
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wasDerivedFrom
64c9bf184ba26fd67f14bdd1d275a3dd0f9b6413
P2860
WNT1 mutations in early-onset osteoporosis and osteogenesis imperfecta.