Cargando…
RBM20 mutations in left ventricular non‐compaction cardiomyopathy
Autores principales: | Gaertner, Anna, Klauke, Bärbel, Brodehl, Andreas, Milting, Hendrik |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2020
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7331358/ https://www.ncbi.nlm.nih.gov/pubmed/32851345 http://dx.doi.org/10.1002/ped4.12184 |
Ejemplares similares
-
Screening for mutations in human cardiomyopathy- is RBM24 a new but rare disease gene?
por: Gaertner, Anna, et al.
Publicado: (2018) -
The Combined Human Genotype of Truncating TTN and RBM20 Mutations Is Associated with Severe and Early Onset of Dilated Cardiomyopathy
por: Gaertner, Anna, et al.
Publicado: (2021) -
A novel desmin (DES) indel mutation causes severe atypical cardiomyopathy in combination with atrioventricular block and skeletal myopathy
por: Schirmer, Ilona, et al.
Publicado: (2017) -
The Desmin (DES) Mutation p.A337P Is Associated with Left-Ventricular Non-Compaction Cardiomyopathy
por: Kulikova, Olga, et al.
Publicado: (2021) -
The Desmin Mutation DES-c.735G>C Causes Severe Restrictive Cardiomyopathy by Inducing In-Frame Skipping of Exon-3
por: Brodehl, Andreas, et al.
Publicado: (2021)