Uncommon IFITM5 mutation...

Annals of Human Genetics 2018 / 07

Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta

Rodriguez Celin, Mercedes, Moosa, Shahida, Fano, Virginia
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Language:
english
Journal:
Annals of Human Genetics
DOI:
10.1111/ahg.12275
Date:
July, 2018
File:
PDF, 1.96 MB
english, 2018
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