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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| Автори: | , , , , , |
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| Формат: | Artigo |
| Мова: | Inglês |
| Опубліковано: |
The Korean Society of Nephrology
2016-06-01
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| Серія: | Kidney Research and Clinical Practice |
| Предмети: | |
| Онлайн доступ: | http://www.sciencedirect.com/science/article/pii/S2211913215300875 |
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