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11. An autopsy case of mitochondrial encephalomyopathy, lactic acidosis and stroke-like episodes (MELAS) with a point mutation of mitochondrial DNA. Terauchi A, Tamagawa K, Morimatsu Y, Kobayashi M, Sano T, Yoda S. Brain Dev; 1996 Oct 02; 18(3):224-9. PubMed ID: 8836506 [Abstract] [Full Text] [Related]
14. Clinicopathological findings of a mitochondrial encephalopathy, lactic acidosis, and stroke-like episodes/Leigh syndrome overlap patient with a novel m.3482A>G mutation in MT-ND1. Hayashi Y, Iwasaki Y, Yoshikura N, Yamada M, Kimura A, Inuzuka T, Miyahara H, Goto Y, Nishino I, Yoshida M, Shimohata T. Neuropathology; 2021 Feb 02; 41(1):84-90. PubMed ID: 33300189 [Abstract] [Full Text] [Related]
16. Expanding the phenotype of SLC25A42-associated mitochondrial encephalomyopathy. Almannai M, Alasmari A, Alqasmi A, Faqeih E, Al Mutairi F, Alotaibi M, Samman MM, Eyaid W, Aljadhai YI, Shamseldin HE, Craigen W, Alkuraya FS. Clin Genet; 2018 May 02; 93(5):1097-1102. PubMed ID: 29327420 [Abstract] [Full Text] [Related]
18. [Mitochondrial diseases]. Pihko H, Suomalainen A, Somer H, Haltia M, Majander A. Duodecim; 1992 May 02; 108(6):578-90. PubMed ID: 1366118 [No Abstract] [Full Text] [Related]
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