5 results on '"Karcagi V"'
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2. Behr's Syndrome is Typically Associated with Disturbed Mitochondrial Translation and Mutations in the C12orf65 Gene
3. Leber's hereditary optic neuropathy - Visual loss caused by a mitochondrial DNA mutation,LEBER-FELE HEREDITAER OPTICUSNEUROPATHIA - VIRUSROMALST OKOZO MITOCHONDRIALIS DNA-MUTACIO
4. Calpain-3 gene defect causing limb gird muscular dystrophy in a Hungarian family,Végtagövi izomdisztrófiát okozó kalpaindefektus egy magyar családban
5. A common mutation (ε1267delG) in congenital myasthenic patients of Gypsy ethnic origin
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