Human Genome Epidemiology Literature Finder
Records 1 - 2 (of 2 Records) |
Query Trace: MELAS Syndrome and ND5[original query] |
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A novel mutation in the mitochondrial MT-ND5 gene in a family with MELAS. The relevance of genetic analysis on targeted tissues. Mitochondrion 2019 10 50 14-18. Panadés-de Oliveira Luísa, Montoya Julio, Emperador Sonia, Ruiz-Pesini Eduardo, Jericó Ivonne, Arenas Joaquín, Hernández-Lain Aurelio, Blázquez Alberto, Martín Miguel Á, Domínguez-González Cristi |
Multisystem mitochondrial diseases due to mutations in mtDNA-encoded subunits of complex I. BMC pediatrics 2020 1 20 (1): 41. Danhelovska Tereza, Kolarova Hana, Zeman Jiri, Hansikova Hana, Vaneckova Manuela, Lambert Lukas, Kucerova-Vidrova Vendula, Berankova Kamila, Honzik Tomas, Tesarova Marke |
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- Page last updated:Apr 29, 2024
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