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mtDNA Depletion Syndrome (Myopathic) — Gene Therapy & Clinical Trials | FollowGene
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mtDNA Depletion Syndrome (Myopathic)
mtDNA Depletion Syndrome (Myopathic)
Prevalence:
1/200000
mitochondrial
Official
·
OMIM:609560
Official
·
ORPHA254875
Myopathic mitochondrial DNA depletion syndrome due to TK2 gene mutations.
Associated Genes
TK2
Thymidine Kinase 2
Chromosome 16
Autosomal Recessive