Identification of mutations in the repeated part of the autosomal dominant polycystic kidney disease type 1 gene, PKD1, by long-range PCR.

Lignende værker

• Autosomal dominant polycystic kidney disease unlinked to the PKD1 and PKD2 loci presenting as familial cerebral aneurysm
  af: MCCONNELL, R, et al.
  Udgivet: (2001)
• PKD1 and PKD2 mutations in Slovenian families with autosomal dominant polycystic kidney disease
  af: Vouk, Katja, et al.
  Udgivet: (2006)
• Autosomal Dominant Polycystic Kidney Disease: Presence of Hypomorphic Alleles in PKD1 Gene
  af: Pandita, S., et al.
  Udgivet: (2018)
• Comprehensive PKD1 and PKD2 Mutation Analysis in Prenatal Autosomal Dominant Polycystic Kidney Disease
  af: Audrézet, Marie-Pierre, et al.
  Udgivet: (2016)
• Novel Mutations in the PKD1 and PKD2 Genes of Chinese Patients with Autosomal Dominant Polycystic Kidney Disease
  af: Dechao Xu, et al.
  Udgivet: (2018-03-01)