Prevalence of maternally inherited diabetes and deafness in diabetic populations in the Netherlands

Diabetologia

Volumn 37, Issue 11, 1994, Pages 1169-1170

  Maassen, J A ^a  

^a Department of Medical Biochemistry ^*  (Netherlands)

Author keywords

[No Author keywords available]

Indexed keywords

ADULT; CONTROLLED STUDY; DIABETES MELLITUS; FEMALE; HEARING IMPAIRMENT; HEREDITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; PRIORITY JOURNAL;

ADULT; DEAFNESS; DIABETES MELLITUS, NON-INSULIN-DEPENDENT; DNA, MITOCHONDRIAL; FEMALE; GROWTH HORMONE; HUMAN; MALE; NETHERLANDS; PEDIGREE; POINT MUTATION; PREVALENCE; RNA, TRANSFER, LEU;

EID: 0027996170     PISSN: 0012186X     EISSN: 14320428     Source Type: Journal    
DOI: 10.1007/BF00418385     Document Type: Letter

References (6)

1. Mutation in mitochondrial tRNALeu(UUR) gene in a large pedigree with maternally transmitted type II diabetes mellitus and deafness
2. Mitochondrial diabetes mellitus: prevalence and clinical characterization of diabetes due to mitochondrial tRNALeu(UUR) gene mutation in Japanese patients
3. A subtype of diabetes mellitus associated with a mutation in the mitochondrial gene
4. Maternally inherited diabetes and deafness (MIDD) is a distinct subtype of diabetes and associates with a single point mutation in the mitochondrial tRNALeu(UUR) gene
5. Prevalence of mitochondrial gene mutations in families with diabetes mellitus
6. Hypothalamic GH deficiency and galastic seizures in a 10-year-old girl with MELAS