A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene

We report a neonatal patient with hypertrophic cardiomyopathy (HCM), lactic acidosis and isolated complex I deficiency. Using a customized next-generation sequencing panel, we identified a novel hemizygous variant c.338G>A in the X-linked NDUFB11 gene that encodes the NADH: ubiquinone oxidoreduct...

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Detalles Bibliográficos
Autores principales: Amate-García, Guillermo, Ballesta-Martínez, María Juliana, Serrano-Lorenzo, Pablo, Garrido-Moraga, Rocío, González-Quintana, Adrián, Blázquez, Alberto, Rubio, Juan C., García-Consuegra, Inés, Arenas, Joaquín, Ugalde, Cristina, Morán, María, Guillén-Navarro, Encarnación, Martín, Miguel A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865986/
https://www.ncbi.nlm.nih.gov/pubmed/36675256
http://dx.doi.org/10.3390/ijms24021743

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9865986/
https://www.ncbi.nlm.nih.gov/pubmed/36675256
http://dx.doi.org/10.3390/ijms24021743

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