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Academic Journal

Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families.

  • Authors : Al-Hamed MH; Department of Genetics, King Faisal Specialist Hospital and Research Centre, P. O. Box 3354, Riyadh, 11211, Saudi Arabia.; Alsahan N

Subjects: Polycystic Kidney, Autosomal Dominant/Polycystic Kidney, Autosomal Dominant/Polycystic Kidney, Autosomal Dominant/*genetics ; TRPP Cation Channels/TRPP Cation Channels/TRPP Cation Channels/*genetics; Age of Onset

  • Source: Pediatric nephrology (Berlin, Germany) [Pediatr Nephrol] 2019 Sep; Vol. 34 (9), pp. 1615-1623. Date of Electronic Publication: 2019 May 11.Publisher: Springer International Country of Publication: Germany NLM ID: 8708728 Publication Model: Print-Electronic Cited Medium: Internet ISSN:

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