Mitochondrial gene variation in type 2 diabetes mellitus: detection of a novel mutation associated with maternally inherited diabetes in a Chinese family.

Ma, L; Wang, H; Chen, J; Jin, W; Liu, L; Ban, B; Shen, J; Hua, Z; Chai, J

Ma, L; Wang, H; Chen, J; Jin, W; Liu, L; Ban, B; Shen, J; Hua, Z; Chai, J.

Affiliation

Ma L; Department of Endocrinology, First Affiliated Hospital of Nanjing Medical University, Nanjing 210029, China. ljma@jlonline.com

Chin Med J (Engl) ; 113(2): 111-6, 2000 Feb.

Article in En | MEDLINE | ID: mdl-11775531

Subject(s)

DNA, Mitochondrial/genetics; Diabetes Mellitus, Type 2/genetics; Adult; Aged; Amino Acid Substitution; Base Sequence; China; DNA/chemistry; DNA/genetics; DNA Mutational Analysis; Diabetes Mellitus, Type 2/pathology; Family Health; Female; Genetic Variation; Humans; Male; Middle Aged; Molecular Sequence Data; Mutation; Pedigree; Point Mutation; Polymorphism, Single-Stranded Conformational; RNA, Transfer, Leu/genetics; Sequence Alignment; Sequence Homology, Nucleic Acid

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Collection: 01-internacional Database: MEDLINE Main subject: DNA, Mitochondrial / Diabetes Mellitus, Type 2 Type of study: Diagnostic_studies / Risk_factors_studies Limits: Adult / Aged / Female / Humans / Male / Middle aged Country/Region as subject: Asia Language: En Journal: Chin Med J (Engl) Year: 2000 Document type: Article Affiliation country: China Country of publication: China

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