Whole exome sequencing reveals a homozygous C1QBP deletion as the cause of progressive external ophthalmoplegia and multiple mtDNA deletions
School for Mental Health and Neuroscience (MHeNS), Maastricht University, Maastricht, the NetherlandsDepartment of Toxicogenomics, Clinical Genomics Unit, Maastricht University, Maastricht, the NetherlandsSchool for Oncology and Developmental Biology (GROW), Maastricht University, Maastricht, the Netherlands
留言 (0)