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Reference15 articles.
1. Carrera P, Calzavara S, Magistroni R, den Dunnen JT, Rigo F, Stenirri S et al (2016) Deciphering variability of PKD1 and PKD2 in an Italian cohort of 643 patients with autosomal dominant polycystic kidney disease (ADPKD). Sci Rep 8(6):30850. https://doi.org/10.1038/srep30850
2. Gumus E, Tuncez E, Oz O, Saka GM (2021) Clinical and exome sequencing findings in seven children with Bardet-Biedl syndrome from Turkey. Ann Hum Genet 85(1):27–36. https://doi.org/10.1111/ahg.12401
3. Harris PC, Rossetti S (2010) Molecular diagnostics for autosomal dominant polycystic kidney disease. Nat Rev Nephrol 6(4):197–206. https://doi.org/10.1038/nrneph.2010.18
4. Harris PC, Torres VE. Polycystic Kidney Disease, Autosomal Dominant. 2002 Jan 10 [Updated 2022 Sep 29]. In: Adam MP, Everman DB, Mirzaa GM, et al., (eds). GeneReviews®. Seattle (WA): University of Washington, Seattle; 1993–2022
5. Jin M, Xie Y, Chen Z, Liao Y, Li Z, Hu P et al (2016) System analysis of gene mutations and clinical phenotype in Chinese patients with autosomal-dominant polycystic kidney disease. Sci Rep 26(6):35945. https://doi.org/10.1038/srep35945