Mitochondrial Multiorgan Disorder Syndrome (Mimods) Due To Mutations In The Slc25a46 Gene
Resumen
In a recent article, Braunisch et al. reported about 4 patients
(VI-5, VI-4, II-3, II-4) with pontocerebellar hypoplasia
(PCH) due to mutations in the SLC25A46 gene1. We have
the following comments and concerns
How to Cite
Josef Finsterer, MD, PhD, Sinda Zarrouk-Mahjoub, PhD (2018). Mitochondrial Multiorgan Disorder Syndrome (Mimods) Due To Mutations In The Slc25a46 Gene. Journal of Medical Biomedical and Applied Sciences , Vol. 6 Núm. 6 (2018) , 66 . https://doi.org/10.15520/jmbas.v6i6.119