Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta

2018 | journal article. A publication with affiliation to the University of Göttingen.

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​Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta​
Rodriguez Celin, M.; Moosa, S.   & Fano, V.​ (2018) 
Annals of Human Genetics, 82(6) pp. 477​-481​.​ DOI: https://doi.org/10.1111/ahg.12275 

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Authors
Rodriguez Celin, Mercedes; Moosa, Shahida ; Fano, Virginia
Issue Date
2018
Journal
Annals of Human Genetics 
ISSN
0003-4800
Language
English

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