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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Autori principali:	Mona Entezam, Mohammad Reza Khatami, Fereshteh Saddadi, Mohsen Ayati, Jamshid Roozbeh, Mohammad Keramatipour
Natura:	Artigo
Lingua:	Inglês
Pubblicazione:	The Korean Society of Nephrology 2016-06-01
Serie:	Kidney Research and Clinical Practice
Soggetti:	Autosomal dominant polycystic kidney disease Linkage analysis Mutation screening Recombination
Accesso online:	http://www.sciencedirect.com/science/article/pii/S2211913215300875
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