Human Genome Epidemiology Literature Finder
Records 1 - 3 (of 3 Records) |
Query Trace: SLC25A4[original query] |
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Association of novel POLG mutations and multiple mitochondrial DNA deletions with variable clinical phenotypes in a Spanish population. Archives of neurology 2006 1 63 (1): 107-11. González-Vioque Emiliano, Blázquez Alberto, Fernández-Moreira Daniel, Bornstein Belén, Bautista Juan, Arpa Javier, Navarro Carmen, Campos Yolanda, Fernández-Moreno Miguel A, Garesse Rafael, Arenas Joaquin, Martín Miguel |
Mitochondrial pathology in inclusion body myositis. Neuromuscular disorders : NMD 2015 Apr 25 (4): 281-8. Lindgren Ulrika, Roos Sara, Hedberg Oldfors Carola, Moslemi Ali-Reza, Lindberg Christopher, Oldfors Ande |
Molecular analysis of inherited cardiomyopathy using next generation semiconductor sequencing technologies. Journal of translational medicine 2018 9 16 (1): 241. Lu Chaoxia, Wu Wei, Liu Fang, Yang Kunqi, Li Jiacheng, Liu Yaping, Wang Rongrong, Si Nuo, Gao Peng, Liu Yongtai, Zhang Shuyang, Zhang X |
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