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Q42630989-3ECD1BAF-4413-4B3B-9BDF-3EB58FD2A0E9
Q42630989-3ECD1BAF-4413-4B3B-9BDF-3EB58FD2A0E9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42630989-3ECD1BAF-4413-4B3B-9BDF-3EB58FD2A0E9
A nonclassical IFITM5 mutation located in the coding region causes severe osteogenesis imperfecta with prenatal onset.
P2860
Q42630989-3ECD1BAF-4413-4B3B-9BDF-3EB58FD2A0E9
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42630989-3ECD1BAF-4413-4B3B-9BDF-3EB58FD2A0E9
rank
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type
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Statement
wasDerivedFrom
862c4bc75400cf5952ae6966c213042eac2ce5a6
P2860
Genetic heterogeneity in osteogenesis imperfecta.