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Q52351034-F80E1520-AA9D-447B-BDB1-BC35ECD10B8A
Q52351034-F80E1520-AA9D-447B-BDB1-BC35ECD10B8A
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Statement
http://www.wikidata.org/entity/statement/Q52351034-F80E1520-AA9D-447B-BDB1-BC35ECD10B8A
Complex heterozygous WNT1 mutation in severe recessive osteogenesis imperfecta of a Chinese patient.
P2860
Q52351034-F80E1520-AA9D-447B-BDB1-BC35ECD10B8A
BestRank
Statement
http://www.wikidata.org/entity/statement/Q52351034-F80E1520-AA9D-447B-BDB1-BC35ECD10B8A
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Statement
wasDerivedFrom
37d624e7bf17185596fea2d72a480ccc9ef7ac82
P2860
Variable brain phenotype primarily affects the brainstem and cerebellum in patients with osteogenesis imperfecta caused by recessive WNT1 mutations