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Q42630989-0A6CB693-CEFD-4DBD-B3B4-B611FCD31F82
Q42630989-0A6CB693-CEFD-4DBD-B3B4-B611FCD31F82
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42630989-0A6CB693-CEFD-4DBD-B3B4-B611FCD31F82
A nonclassical IFITM5 mutation located in the coding region causes severe osteogenesis imperfecta with prenatal onset.
P2860
Q42630989-0A6CB693-CEFD-4DBD-B3B4-B611FCD31F82
BestRank
Statement
http://www.wikidata.org/entity/statement/Q42630989-0A6CB693-CEFD-4DBD-B3B4-B611FCD31F82
rank
NormalRank
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Statement
wasDerivedFrom
862c4bc75400cf5952ae6966c213042eac2ce5a6
P2860
De novo mutations in human genetic disease.