Identification of novel mutations and risk assessment of Han Chinese patients with autosomal dominant polycystic kidney disease
Author:
Affiliation:
1. Institute of Clinical Laboratory Science, Jinling Hospital, School of MedicineNanjing University Nanjing China
2. National Clinical Research Center of Kidney Diseases, Jinling Hospital, School of MedicineNanjing University Nanjing China
Publisher
Wiley
Subject
Nephrology,General Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/nep.13270
Reference34 articles.
1. Polycystic kidney disease;Wilson PD;N. Engl. J. Med.,2004
2. Polycystic kidney disease;Harris PC;Annu. Rev. Med.,2009
3. Autosomal dominant polycystic kidney disease;Torres VE;Lancet,2007
4. Evaluation of ultrasonographic diagnostic criteria for autosomal dominant polycystic kidney disease 1;Ravine D;Lancet,1994
5. A novel mutation of the SLC25A13 gene in a Chinese patient with citrin deficiency detected by target next‐generation sequencing;Liu G;Gene,2014
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