Associated Papers
A Novel Mutation Associated with Neonatal Lethal Cardiomyopathy Leads to an Alternative Transcript Expression in the X-Linked Complex I NDUFB11 Gene.
Amate-García G et al.
International Journal of Molecular Sciences, 2023
An Overview of Mitochondrial Protein Defects in Neuromuscular Diseases.
Marra F et al.
Biomolecules, 2021
Diverse phenotype in patients with complex I deficiency due to mutations in NDUFB11.
Reinson K et al.
European Journal of Medical Genetics, 2019
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