Chargement en cours...
Structure of GroEL in Complex with an Early Folding Intermediate of Alanine Glyoxylate Aminotransferase
Primary hyperoxaluria type 1 is a rare autosomal recessive disease caused by mutations in the alanine glyoxylate aminotransferase gene (AGXT). We have previously shown that P11L and I340M polymorphisms together with I244T mutation (AGXT-LTM) represent a conformational disease that could be amenable...
Enregistré dans:
| Auteurs principaux: | , , , , , , |
|---|---|
| Format: | Artigo |
| Langue: | Inglês |
| Publié: |
American Society for Biochemistry and Molecular Biology
2010
|
| Sujets: | |
| Accès en ligne: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2825432/ https://ncbi.nlm.nih.gov/pubmed/20056599 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1074/jbc.M109.062471 |
| Tags: |
Ajouter un tag
Pas de tags, Soyez le premier à ajouter un tag!
|