Uncommon IFITM5 mutation associated with severe skeletal deformity in osteogenesis imperfecta.
| Autor: | Rodriguez Celin, Mercedes1 mercedesrodriguezcelin@gmail.com, Moosa, Shahida2, Fano, Virginia1 |
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| Zdroj: | Annals of Human Genetics. Nov2018, Vol. 82 Issue 6, p477-481. 5p. |
| Databáze: | Academic Search Ultimate |
| Externí odkaz: |
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