A carregar...
Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitus
Permanent neonatal diabetes mellitus (PNDM) is a rare disorder usually presenting within 6 months of birth. Although several genes have been linked to this disorder, in almost half the cases documented in Italy, the genetic cause remains unknown. Because the Akita mouse bearing a mutation in the Ins...
Na minha lista:
Main Authors: | , , , , , , , , , , , , , , , , , , |
---|---|
Formato: | Artigo |
Idioma: | Inglês |
Publicado em: |
American Society for Clinical Investigation
2008
|
Assuntos: | |
Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2350430/ https://ncbi.nlm.nih.gov/pubmed/18451997 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1172/JCI33777 |
Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|