Bialleleic PKD1 mutations underlie early-onset autosomal dominant polycystic kidney disease in Saudi Arabian families-Reference-Cited by-同舟云学术

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

Published:2019-05-11 Issue:9 Volume:34 Page:1615-1623
ISSN:0931-041X
Container-title:Pediatric Nephrology
language:en
Short-container-title:Pediatr Nephrol

Author:

Al-Hamed Mohamed H.^ORCID,Alsahan Nada,Rice Sarah J.,Edwards Noel,Nooreddeen Eman,Alotaibi Maha,Kurdi Wesam,Alnemer Maha,Altaleb Naderah,Ali Wafa,Al-Numair Nouf,Almejaish Najd,Sayer John A.,Imtiaz Faiqa

Publisher

Springer Science and Business Media LLC

Subject

Nephrology,Pediatrics, Perinatology, and Child Health

Link

http://link.springer.com/content/pdf/10.1007/s00467-019-04267-x.pdf

Reference37 articles.

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2. Hildebrandt F, Otto E (2005) Cilia and centrosomes: a unifying pathogenic concept for cystic kidney disease? Nat Rev Genet 6:928–940

3. Igarashi P, Somlo S (2002) Genetics and pathogenesis of polycystic kidney disease. J Am Soc Nephrol 13:2384–2398

4. Hulten M (1988) Linkage heterogeneity in autosomal dominant polycystic kidney disease. Lancet 2:451–452

5. Kimberling WJ, Fain PR, Kenyon JB, Goldgar D, Sujansky E, Gabow PA (1988) Linkage heterogeneity of autosomal dominant polycystic kidney disease. N Engl J Med 319:913–918

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