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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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Principais autores: Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour
Format: Artigo
Sprog:Inglês
Udgivet: The Korean Society of Nephrology 2016-06-01
Serier:Kidney Research and Clinical Practice
Fag:
Autosomal dominant polycystic kidney disease
Linkage analysis
Mutation screening
Recombination
Online adgang:http://www.sciencedirect.com/science/article/pii/S2211913215300875
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