Cargando…
Correction to: Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
Autores principales: | Inoue, Tomohiko, Nagano, China, Matsuo, Masafumi, Yamamura, Tomohiko, Sakakibara, Nana, Horinouchi, Tomoko, Shibagaki, Yugo, Ichikawa, Daisuke, Aoto, Yuya, Ishiko, Shinya, Ishimori, Shingo, Rossanti, Rini, Iijima, Kazumoto, Nozu, Kandai |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Singapore
2021
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8038978/ https://www.ncbi.nlm.nih.gov/pubmed/33721133 http://dx.doi.org/10.1007/s10157-021-02041-8 |
Ejemplares similares
-
Functional analysis of suspected splicing variants in CLCN5 gene in Dent disease 1
por: Inoue, Tomohiko, et al.
Publicado: (2020) -
Pathogenic evaluation of synonymous COL4A5 variants in X‐linked Alport syndrome using a minigene assay
por: Horinouchi, Tomoko, et al.
Publicado: (2020) -
Comparison between conventional and comprehensive sequencing approaches for genetic diagnosis of Alport syndrome
por: Yamamura, Tomohiko, et al.
Publicado: (2019) -
Comprehensive genetic diagnosis of Japanese patients with severe proteinuria
por: Nagano, China, et al.
Publicado: (2020) -
Determination of the pathogenicity of known COL4A5 intronic variants by in vitro splicing assay
por: Horinouchi, Tomoko, et al.
Publicado: (2019)