Novel mutations of the PKD1 gene in Korean patients with autosomal dominant polycystic kidney disease
β Scribed by Un Kyung Kim; Dong Kyu Jin; Curie Ahn; Jae Hyun Shin; Kyu Beck Lee; Sung Han Kim; Jae Jin Chae; Dae Yeon Hwang; Jung Geon Lee; Yong Namkoong; Chung Choo Lee
- Book ID
- 117768015
- Publisher
- Elsevier Science
- Year
- 2000
- Tongue
- English
- Weight
- 216 KB
- Volume
- 432
- Category
- Article
- ISSN
- 1383-5726
No coin nor oath required. For personal study only.
π SIMILAR VOLUMES
## Paalman Autosomal dominant polycystic kidney disease (ADPKD) is a common genetic renal disorder (incidence, 1:1,000). The mutation of PKD1 is thought to account for 85% of ADPKD. Although a considerable number of studies on PKD1 mutation have been published recently, most of them concern Caucasi
## 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
## Communicated by Mark H. Paalman Autosomal dominant polycystic kidney disease (ADPKD) is a genetically heterogeneous disease caused by mutations in at least three different loci. Mutations in the PKD2 gene are responsible for approximately 15% of the cases of the disease. We have screened 14 Cze