Alterações na homeostase redox e do retículo endoplasmático: mecanismos associados à lipodistrofia generalizada congênita do tipo 2
Congenital generalized lipodystrophy (CGL) type 2 consists of a rare autosomal recessive syndrome characterized by almost complete lack of body fat at birth. CGL, genetically caused by loss-of-function mutations in the two alleles of the BSCL2 gene, was phenotypically characterized by hypertrigly...
Gorde:
| Egile nagusia: | |
|---|---|
| Beste egile batzuk: | |
| Formatua: | Dissertação |
| Hizkuntza: | pt_BR |
| Argitaratua: |
Brasil
|
| Gaiak: | |
| Sarrera elektronikoa: | https://repositorio.ufrn.br/jspui/handle/123456789/27009 |
| Etiketak: |
Etiketa erantsi
Etiketarik gabe, Izan zaitez lehena erregistro honi etiketa jartzen!
|
Izan zaitez lehena ohar bat uzten!