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

Παρόμοια τεκμήρια

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