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Q36983068-4AD8D277-11D6-4C51-96B2-F2F29839A868
Q36983068-4AD8D277-11D6-4C51-96B2-F2F29839A868
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-4AD8D277-11D6-4C51-96B2-F2F29839A868
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations
P2860
Q36983068-4AD8D277-11D6-4C51-96B2-F2F29839A868
BestRank
Statement
http://www.wikidata.org/entity/statement/Q36983068-4AD8D277-11D6-4C51-96B2-F2F29839A868
rank
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type
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Statement
wasDerivedFrom
2b14afd9bf6378632459a1e3a5b73bf1cdaf81a4
P2860
Mutations in patients with osteogenesis imperfecta from consanguineous Indian families.