Frequency and clinical features of patients with sensorineural hearing loss associated with the A3243G mutation of the mitochondrial DNA in otorhinolaryngic clinics

Journal of Human Genetics

Volumn 46, Issue 10, 2001, Pages 595-599

  Nagata, H ^a   Kumahara, K ^a   Tomemori, T ^a   Arimoto, Y ^a   Isoyama, K ^a   Yoshida, K ^a   Konno, A ^a  

^a CHIBA UNIVERSITY   (Japan)

Author keywords

Cardiomyopathy; Diabetes mellitus; Genetic test; Mitochondrial DNA; Point mutation; Sensorineural hearing loss

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; ARTICLE; CARDIOMYOPATHY; CLINICAL FEATURE; CONTROLLED STUDY; DIABETES MELLITUS; DISEASE ASSOCIATION; EXTRACHROMOSOMAL INHERITANCE; FAMILY HISTORY; FEMALE; GENE FREQUENCY; GENE MUTATION; HUMAN; HUMAN CELL; MAJOR CLINICAL STUDY; MALE; MUTATION RATE; ONSET AGE; OTORHINOLARYNGOLOGY; PERCEPTION DEAFNESS;

ADOLESCENT; ADULT; AGE OF ONSET; CHILD; DIABETES COMPLICATIONS; DIABETES MELLITUS; DNA, MITOCHONDRIAL; FAMILY HEALTH; FEMALE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MUTATION; RNA, TRANSFER, LEU;

EID: 0034758460     PISSN: 14345161     EISSN: None     Source Type: Journal    
DOI: 10.1007/s100380170027     Document Type: Article

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