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Association of mutation position in polycystic kidney disease 1 (PKD1) gene and development of a vascular phenotype

โœ Scribed by Sandro Rossetti; Dominique Chauveau; Vickie Kubly; Jeffrey M Slezak; Anand K Saggar-Malik; York Pei; Albert CM Ong; Fiona Stewart; Michael L Watson; Erik J Bergstralh; Christopher G Winearls; Vicente E Torres; Peter C Harris


Book ID
117284016
Publisher
The Lancet
Year
2003
Tongue
English
Weight
106 KB
Volume
361
Category
Article
ISSN
0140-6736

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## Communicated by Michel Goossens Autosomal dominant polycystic kidney disease (ADPKD) is a common disorder mostly characterized by cyst formation in kidney tubules. The majority of ADPKD cases is caused by mutations in the PKD1 gene, but no prevalent mutation has been reported. By heteroduplex a