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Single-fiber analysis of mitochondrial A3243G mutation in four different phenotypes.
Koga, Y; Koga, A; Iwanaga, R; Akita, Y; Tubone, J; Matsuishi, T; Takane, N; Sato, Y; Kato, H.
Affiliation
  • Koga Y; Department of Pediatrics and Child Health, Kurume University School of Medicine, Fukuoka, Japan. yasukoga@med.kurume-u.ac.jp
Acta Neuropathol ; 99(2): 186-90, 2000 Feb.
Article in En | MEDLINE | ID: mdl-10672326
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Leigh Disease / Point Mutation / Ophthalmoplegia, Chronic Progressive External / MELAS Syndrome / Muscle, Skeletal / Muscle Fibers, Skeletal / Diabetes Mellitus Limits: Adult / Child / Humans / Middle aged Language: En Journal: Acta Neuropathol Year: 2000 Document type: Article Affiliation country: Japón
Search on Google
Add to My VHL
Print
XML
PubMed Links

Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Leigh Disease / Point Mutation / Ophthalmoplegia, Chronic Progressive External / MELAS Syndrome / Muscle, Skeletal / Muscle Fibers, Skeletal / Diabetes Mellitus Limits: Adult / Child / Humans / Middle aged Language: En Journal: Acta Neuropathol Year: 2000 Document type: Article Affiliation country: Japón