Coenzyme Q10 deficiency due to a COQ4 gene defect causes childhood-onset spinocerebellar ataxia and stroke-like episodes

Primary coenzyme Q10 deficiency-7 is caused by homozygous or compound heterozygous mutations in the COQ4 gene. Until now 12 patients have been reported, most presenting with a lethal infantile phenotype with encephalopathy, epilepsy and cardiomyopathy. We report on a new phenotype of COQ4 deficiency...

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Detalles Bibliográficos
Autores principales: Bosch, Annet M., Kamsteeg, Erik-Jan, Rodenburg, Richard J., van Deutekom, Arend W., Buis, Dennis R., Engelen, Marc, Cobben, Jan-Maarten
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2018
Materias:
Case Report
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138878/
https://www.ncbi.nlm.nih.gov/pubmed/30225196
http://dx.doi.org/10.1016/j.ymgmr.2018.09.002

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6138878/
https://www.ncbi.nlm.nih.gov/pubmed/30225196
http://dx.doi.org/10.1016/j.ymgmr.2018.09.002

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