Update in molecular genetics: mitochondrial energy transduction disorders.

Marzuki, S; Sudoyo, H; Lertrit, P

Marzuki, S; Sudoyo, H; Lertrit, P.

Southeast Asian J Trop Med Public Health ; 1995 ; 26 Suppl 1(): 155-61

Article in English | IMSEAR | ID: sea-34176

Subject(s)

Asia, Southeastern; Chromosomes, Human; DNA, Mitochondrial/genetics; Female; Genetic Diseases, Inborn/genetics; Humans; MELAS Syndrome/genetics; MERRF Syndrome/genetics; Male; Mitochondria/metabolism; Mitochondrial Encephalomyopathies/genetics; Mitochondrial Myopathies/genetics; Optic Atrophies, Hereditary/genetics; Pedigree; Point Mutation; Polymorphism, Restriction Fragment Length

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Full text: Available Index: IMSEAR (South-East Asia) Main subject: Pedigree / Asia, Southeastern / Polymorphism, Restriction Fragment Length / Female / Humans / Male / DNA, Mitochondrial / Optic Atrophies, Hereditary / Chromosomes, Human / Point Mutation Country/Region as subject: Asia Language: English Journal: Southeast Asian J Trop Med Public Health Year: 1995 Type: Article

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