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CPEO and carnitine deficiency overlapping in MELAS syndrome.
Hsu CC, Chuang YH, Tsai JL, Jong HJ, Shen YY, Huang HL, Chen HL, Lee HC, Pang CY, Wei YH, et al. Hsu CC, et al. Acta Neurol Scand. 1995 Sep;92(3):252-5. doi: 10.1111/j.1600-0404.1995.tb01697.x. Acta Neurol Scand. 1995. PMID: 7484081
A specific 4977-bp deletion of mitochondrial DNA in human ageing skin.
Yang JH, Lee HC, Lin KJ, Wei YH. Yang JH, et al. Arch Dermatol Res. 1994;286(7):386-90. doi: 10.1007/BF00371798. Arch Dermatol Res. 1994. PMID: 7818280
MELAS syndrome: correlation between clinical features and molecular genetic analysis.
Liou CW, Huang CC, Chee EC, Jong YJ, Tsai JL, Pang CY, Lee HC, Wei YH. Liou CW, et al. Acta Neurol Scand. 1994 Nov;90(5):354-9. doi: 10.1111/j.1600-0404.1994.tb02737.x. Acta Neurol Scand. 1994. PMID: 7887136
Human skin mitochondrial DNA deletions associated with light exposure.
Pang CY, Lee HC, Yang JH, Wei YH. Pang CY, et al. Arch Biochem Biophys. 1994 Aug 1;312(2):534-8. doi: 10.1006/abbi.1994.1342. Arch Biochem Biophys. 1994. PMID: 8037468
MELAS syndrome with mitochondrial tRNA(Leu(UUR)) gene mutation in a Chinese family.
Huang CC, Chen RS, Chen CM, Wang HS, Lee CC, Pang CY, Hsu HS, Lee HC, Wei YH. Huang CC, et al. J Neurol Neurosurg Psychiatry. 1994 May;57(5):586-9. doi: 10.1136/jnnp.57.5.586. J Neurol Neurosurg Psychiatry. 1994. PMID: 8201329 Free PMC article.
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