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...
Enregistré dans:
Auteur principal: | |
---|---|
Autres auteurs: | |
Format: | Dissertação |
Langue: | pt_BR |
Publié: |
Brasil
|
Sujets: | |
Accès en ligne: | https://repositorio.ufrn.br/jspui/handle/123456789/27009 |
Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|