Co-existence of m.10663T>C Mutation with Haplogroup L3f1b Background in a Patient with LHON
| Autor: | Majed Alkharashi, Abdullah S. Al-Kharashi, Altaf A. Kondkar, Khaled K. Abu-Amero, Majed Al-Obailan |
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| Rok vydání: | 2016 |
| Předmět: |
Male
0301 basic medicine Genetics Mitochondrial DNA medicine.diagnostic_test business.industry Mutation Missense NADH Dehydrogenase Optic Atrophy Hereditary Leber General Medicine Bioinformatics Haplogroup Pedigree Young Adult 03 medical and health sciences 030104 developmental biology Neurology Mutation (genetic algorithm) Humans Medicine Female Neurology (clinical) business Genetic testing |
| Zdroj: | Canadian Journal of Neurological Sciences / Journal Canadien des Sciences Neurologiques. 43:332-333 |
| ISSN: | 2057-0155 0317-1671 |
| DOI: | 10.1017/cjn.2015.345 |
| Databáze: | OpenAIRE |
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