A carregar...
PKD2 mutation in an Iranian autosomal dominant polycystic kidney disease family with misleading linkage analysis data()
BACKGROUND: Autosomal dominant polycystic kidney disease (ADPKD) is the most common genetic renal disorder caused by mutation in 2 genes PKD1 and PKD2. Thus far, no mutation is identified in approximately 10% of ADPKD families, which can suggest further locus heterogeneity. Owing to the complexity o...
Na minha lista:
| Publicado no: | Kidney Res Clin Pract |
|---|---|
| Main Authors: | , , , , , |
| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
Elsevier
2016
|
| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4919558/ https://ncbi.nlm.nih.gov/pubmed/27366664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1016/j.krcp.2016.02.003 |
| Tags: |
Adicionar Tag
Sem tags, seja o primeiro a adicionar uma tag!
|