Presence of De Novo Mutations in Autosomal Dominant Polycystic Kidney Disease Patients Without Family History-Reference-Cited by-同舟云学术

Presence of De Novo Mutations in Autosomal Dominant Polycystic Kidney Disease Patients Without Family History

Published:2008-12 Issue:6 Volume:52 Page:1042-1050
ISSN:0272-6386
Container-title:American Journal of Kidney Diseases
language:en
Short-container-title:American Journal of Kidney Diseases

Author:

Reed Berenice,McFann Kim,Kimberling William J.,Pei York,Gabow Patricia A.,Christopher Karen,Petersen Eric,Kelleher Catherine,Fain Pamela R.,Johnson Ann,Schrier Robert W.

Publisher

Elsevier BV

Subject

Nephrology

Reference31 articles.

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3. Mutation detection of PKD1 identifies a novel mutation common to three families with aneurysms and/or very-early-onset disease;Watnick;Am J Hum Genet,1999

4. The position of the polycystic kidney disease 1 (PKD1) gene mutation correlates with the severity of renal disease;Rossetti;J Am Soc Nephrol,2000

5. Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype;Rossetti;Lancet,2003

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