Cargando…
A Schematic Approach to Defining the Prevalence of COL VI Variants in Five Years of Next-Generation Sequencing
Objective: To define the prevalence of variants in collagen VI genes through a next-generation sequencing (NGS) approach in undiagnosed patients with suspected neuromuscular disease and to propose a diagnostic flowchart to assess the real pathogenicity of those variants. Methods: In the past five ye...
Autores principales: | Marinella, Gemma, Astrea, Guja, Buchignani, Bianca, Cassandrini, Denise, Doccini, Stefano, Filosto, Massimiliano, Galatolo, Daniele, Gallone, Salvatore, Giannini, Fabio, Lopergolo, Diego, Maioli, Maria Antonietta, Magri, Francesca, Malandrini, Alessandro, Mandich, Paola, Mari, Francesco, Massa, Roberto, Mata, Sabrina, Melani, Federico, Moggio, Maurizio, Mongini, Tiziana E., Pasquariello, Rosa, Pegoraro, Elena, Ricci, Federica, Ricci, Giulia, Rodolico, Carmelo, Rubegni, Anna, Siciliano, Gabriele, Sperti, Martina, Ticci, Chiara, Tonin, Paola, Santorelli, Filippo M., Battini, Roberta |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9735635/ https://www.ncbi.nlm.nih.gov/pubmed/36498898 http://dx.doi.org/10.3390/ijms232314567 |
Ejemplares similares
-
Using Cluster Analysis to Overcome the Limits of Traditional Phenotype–Genotype Correlations: The Example of RYR1-Related Myopathies
por: Dosi, Claudia, et al.
Publicado: (2023) -
Expanding the clinical and genetic heterogeneity of SPAX5
por: Dosi, Claudia, et al.
Publicado: (2020) -
Congenital Myopathy as a Phenotypic Expression of CACNA1S Gene Mutation: Case Report and Systematic Review of the Literature
por: Marinella, Gemma, et al.
Publicado: (2023) -
Next-generation sequencing approach to hyperCKemia: A 2-year cohort study
por: Rubegni, Anna, et al.
Publicado: (2019) -
Congenital myopathies: clinical phenotypes and new diagnostic tools
por: Cassandrini, Denise, et al.
Publicado: (2017)