Screening of mitochondrial mutations in Tunisian patients with mitochondrial disorders: an overview study

Medicine & Life Sciences

• Mitochondrial Diseases 100%
• Mutation 44%
• MELAS Syndrome 40%
• Wolfram Syndrome 29%
• Kearns-Sayre Syndrome 28%
• Leigh Disease 26%
• Polymerase Chain Reaction 21%
• Restriction Fragment Length Polymorphisms 17%
• Hearing Loss 16%
• RNA, Transfer, Trp 16%
• Noninsulin-dependent diabetes mellitus with deafness 16%
• RNA, Transfer, Ile 15%
• RNA, Transfer, Val 15%
• RNA, Transfer, Glu 15%
• ribosomal RNA 12S 14%
• Tunisia 11%
• Electron Transport Complex IV 10%
• Hypertrophic Cardiomyopathy 10%
• Deafness 9%
• Muscular Diseases 9%
• Cardiomyopathies 8%
• Genes 7%