Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus

Acta Diabetologica

Volumn 36, Issue 3, 1999, Pages 163-167

  Rigoli, L ^a   Salpietro, D C ^a   Caruso, R A ^a   Chiarenza, A ^a   Barberi, I ^a  

^a UNIVERSITY OF MESSINA   (Italy)

Author keywords

Deafness; Genetics; Maternally inherited diabetes mellitus; Mitochondrial DNA; np 3243 mutation

Indexed keywords

LEUCINE; MITOCHONDRIAL DNA; NUCLEOTIDE; TRANSFER RNA;

ADOLESCENT; ADULT; ARTICLE; CLINICAL ARTICLE; DIABETES MELLITUS; FAMILY STUDY; FEMALE; FOLLOW UP; GENE DELETION; GENE MUTATION; HEARING IMPAIRMENT; HEREDITARY OPTIC ATROPHY; HUMAN; HUMAN TISSUE; INHERITANCE; ITALY; MALE; MENTAL DEFICIENCY; METABOLISM; MOTHER; NON INSULIN DEPENDENT DIABETES MELLITUS; PHENOTYPE; PREVALENCE; PRIORITY JOURNAL; SCHOOL CHILD;

BLOOD GLUCOSE; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; EXTRACHROMOSOMAL INHERITANCE; FEMALE; GLUCOSE TOLERANCE TEST; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MOTHERS; OPTIC ATROPHIES, HEREDITARY; PEDIGREE; POINT MUTATION;

EID: 0033396481     PISSN: 09405429     EISSN: None     Source Type: Journal    
DOI: 10.1007/s005920050161     Document Type: Article

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