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...

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Detalles Bibliográficos
Autores principales: Entezam, Mona, Khatami, Mohammad Reza, Saddadi, Fereshteh, Ayati, Mohsen, Roozbeh, Jamshid, Keramatipour, Mohammad
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2016
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919558/
https://www.ncbi.nlm.nih.gov/pubmed/27366664
http://dx.doi.org/10.1016/j.krcp.2016.02.003

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4919558/
https://www.ncbi.nlm.nih.gov/pubmed/27366664
http://dx.doi.org/10.1016/j.krcp.2016.02.003

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