Importance of searching for mtDNA defects in patients with diabetes and hearing deficit [1]

Diabetologia

Volumn 41, Issue 6, 1998, Pages 740-741

  Paquis Flucklinger, V ^a   Vialettes, B ^a   Vague, P ^a   Canivet, B ^a   Hieronimus, S ^a   Oliver, C ^a   Pellissier, J F ^a   Saunieres, A ^a   Desnuelle, C ^a  

^a UNIVERSITÉ CÔTE D'AZUR   (France)

Author keywords

[No Author keywords available]

Indexed keywords

ADOLESCENT; ADULT; AGED; DIABETES MELLITUS; DISEASE ASSOCIATION; FEMALE; GENE MUTATION; HEARING IMPAIRMENT; HERITABILITY; HUMAN; LETTER; MAJOR CLINICAL STUDY; MALE; NUCLEIC ACID BASE SUBSTITUTION; PERCEPTION DEAFNESS; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL; RESPIRATORY CHAIN; RISK FACTOR; SEX DIFFERENCE;

ADOLESCENT; ADULT; AGED; AGED, 80 AND OVER; CHILD; DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; EXTRACHROMOSOMAL INHERITANCE; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MOTHERS; MUTATION;

EID: 0031812303     PISSN: 0012186X     EISSN: None     Source Type: Journal    
DOI: 10.1007/s001250050978     Document Type: Letter

References (10)