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...
Guardado en:
| Autor principal: | |
|---|---|
| Otros Autores: | |
| Formato: | Dissertação |
| Lenguaje: | pt_BR |
| Publicado: |
Brasil
|
| Materias: | |
| Acceso en línea: | https://repositorio.ufrn.br/jspui/handle/123456789/27009 |
| Etiquetas: |
Agregar Etiqueta
Sin Etiquetas, Sea el primero en etiquetar este registro!
|