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...
Tallennettuna:
| Päätekijä: | |
|---|---|
| Muut tekijät: | |
| Aineistotyyppi: | Dissertação |
| Kieli: | pt_BR |
| Julkaistu: |
Brasil
|
| Aiheet: | |
| Linkit: | https://repositorio.ufrn.br/jspui/handle/123456789/27009 |
| Tagit: |
Lisää tagi
Ei tageja, Lisää ensimmäinen tagi!
|