Mitochondrial D-Loop variation in Leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors
Document title: Mitochondrial D-Loop variation in Leber hereditary neuropathy patients harboring primary G11778A, G3460A, T14484C mutations: J and W haplogroups as high-risk factors
Journal: Archives of medical research
Database: PERIÓDICA
System number: 000257783
ISSN: 0188-4409
Authors: 1

2
Institutions: 1National Institute for Genetic Engineering and Biotechnology, Department of Medical Genetics, Teherán. Irán
2Farabi Eye Hospital, Teherán. Irán
Year:
Season: Nov
Volumen: 37
Number: 8
Pages: 1022-1027
Country: México
Language: Inglés
Document type: Artículo
Approach: Caso clínico, analítico
Disciplines: Medicina
Keyword: Neurología,
Oftalmología,
Genética,
Neuropatía óptica hereditaria de Leber,
Haplogrupos,
ADN mitocondrial,
Mutaciones,
Enfermedad de Leber
Keyword: Medicine,
Neurology,
Ophthalmology,
Leber disease,
Leber hereditary optic neuropathy,
Haplogroups,
Mitochondrial DNA,
Mutations,
Genetics
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