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...
Guardat en:
| Autor principal: | |
|---|---|
| Altres autors: | |
| Format: | Dissertação |
| Idioma: | pt_BR |
| Publicat: |
Brasil
|
| Matèries: | |
| Accés en línia: | https://repositorio.ufrn.br/jspui/handle/123456789/27009 |
| Etiquetes: |
Afegir etiqueta
Sense etiquetes, Sigues el primer a etiquetar aquest registre!
|