Association of the T14709C mutation of mitochondrial DNA with maternally inherited diabetes mellitus and/or deafness in an Italian family [2]

Diabetic Medicine

Volumn 18, Issue 4, 2001, Pages 334-336

  Rigoli, L ^a   Prisco, F ^b   Caruso, R A ^a   Iafusco, D ^b   Ursomanno, G ^b   Zuccarello, D ^a   Ingenito, N ^b   Rigoli, M ^a   Barberi, I ^a  

^a UNIVERSITY OF MESSINA   (Italy)

^b UNIVERSITY OF NAPLES FEDERICO II   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ETHICS; FAMILY STUDY; GENE MUTATION; GENETIC PREDISPOSITION; HEARING IMPAIRMENT; HUMAN; INHERITANCE; INSULIN DEPENDENT DIABETES MELLITUS; LETTER; MATERNAL DIABETES MELLITUS; NON INSULIN DEPENDENT DIABETES MELLITUS; PEDIGREE;

EID: 0034955834     PISSN: 07423071     EISSN: None     Source Type: Journal    
DOI: 10.1046/j.1464-5491.2001.00429-2.x     Document Type: Letter

References (7)

1. Maternally inherited diabetes mellitus: The role of mitochondrial DNA defects
2. Maternally transmitted diabetes and deafness associated with a 10.4 kb mitochondrial DNA pedigree with sensorineural deafness
3. Diabetes mellitus is one of the heterogeneous phenotypic features of a mitochondrial DNA point mutation within the tRNALeu (UUR) gene
4. Mitochondrial DNA mutation at np 3243 in a family with maternally inherited diabetes mellitus
5. Complete mtDNA sequence of a patient in a maternal pedigree with sensorineural deafness
6. Segregation patterns of a novel mutation in the mitochondrial tRNA glutamic acid gene associated with myopathy and diabetes mellitus
7. Mitochondrial DNA mutations and pathogenesis