Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1

Lignende værker

• Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
  af: Inoue, Tomohiko, et al.
  Udgivet: (2020)
• Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
  af: Nagano, China, et al.
  Udgivet: (2020)
• FAT1 biallelic truncating mutation causes a non-syndromic proteinuria in a child
  af: Rossanti, Rini, et al.
  Udgivet: (2020)
• Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay
  af: Horinouchi, Tomoko, et al.
  Udgivet: (2020)
• A case with somatic and germline mosaicism in COL4A5 detected by multiplex ligation-dependent probe amplification in X-linked Alport syndrome
  af: Aoto, Yuya, et al.
  Udgivet: (2020)