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Q37319354-B7C1C3B4-839B-48EF-9868-9C0B7FFF4E09
Q37319354-B7C1C3B4-839B-48EF-9868-9C0B7FFF4E09
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http://www.wikidata.org/entity/statement/Q37319354-B7C1C3B4-839B-48EF-9868-9C0B7FFF4E09
Asymptomatic parental mosaicism for osteogenesis imperfecta associated with a new splice site mutation in COL1A2.
P2860
Q37319354-B7C1C3B4-839B-48EF-9868-9C0B7FFF4E09
BestRank
Statement
http://www.wikidata.org/entity/statement/Q37319354-B7C1C3B4-839B-48EF-9868-9C0B7FFF4E09
rank
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type
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wasDerivedFrom
0cd8335b12921c7f0264169b44ce77f9518b23df
P2860
Recurrence of lethal osteogenesis imperfecta due to parental mosaicism for a dominant mutation in a human type I collagen gene (COL1A1).