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XB-GENEPAGE-978895
Gene Symbol: twnk
Gene Name: twinkle mtDNA helicase
Synonyms:
c10orf2
(
Gene Function: mitochondrial DNA helicase twinkle Protein Function
![]() Interactants:
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Diseases: Disease Ontology: autosomal dominant progressive external ophthalmoplegia with mitochondrial DNA deletions 3
MIM:
PERRAULT SYNDROME 5; PRLTS5
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Expression | Development Stages Embryonic Tissues Adult Tissues | |||||||||||
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