Metreleptin Treatment in a Boy with Congenital Generalized Lipodystrophy due to Homozygous c.465_468delGACT (p.T156Rfs*8) Mutation in the BSCL2 Gene: Results From the First-year.
| Autor: | Özalkak, Şervan1 drservanoz@gmail.com, Demiral, Meliha2, Ünal, Edip3, Taş, Funda Feryal1, Onay, Hüseyin4, Demirbilek, Hüseyin5, Özbek, Mehmet Nuri1 |
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| Zdroj: | Journal of Clinical Research in Pediatric Endocrinology. Sep2023, Vol. 15 Issue 3, p329-333. 5p. |
| Databáze: | Academic Search Ultimate |
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