Genetic features, clinical phenotypes, and prevalence of sensorineural hearing loss associated with the 961delT mitochondrial mutation

Auris Nasus Larynx

Volumn 32, Issue 2, 2005, Pages 119-124

  Kobayashi, Katsuhiko ^a   Oguchi, Tomohiro ^a   Asamura, Kenji ^a   Miyagawa, Maiko ^a   Horai, Satoshi ^b   Abe, Satoko ^c,d   Usami, Shin Ichi ^a  

^a SHINSHU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b GRADUATE UNIVERSITY FOR ADVANCED STUDIES   (Japan)

^c BML   (Japan)

^d Abe ENT Clinic   (Japan)

Author keywords

961delT; Aminoglycoside antibiotics; Hearing impairment; Mitochondria

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT;

ADOLESCENT; ADULT; AGED; AGING; ANAMNESIS; ARTICLE; CHILD; CLINICAL FEATURE; CONTROLLED STUDY; CORRELATION ANALYSIS; DISEASE ASSOCIATION; DISEASE SEVERITY; DRUG INDUCED DISEASE; FAMILY; GENE DELETION; GENE FREQUENCY; GENETIC ANALYSIS; GENETIC ASSOCIATION; HEARING LOSS; HETEROPLASMY; HUMAN; INFANT; INJECTION; MAJOR CLINICAL STUDY; MITOCHONDRIAL GENETICS; NEWBORN; OTOTOXICITY; PATIENT; PERCEPTION DEAFNESS; PHENOTYPE; POINT MUTATION; POPULATION; PREVALENCE; RESTRICTION FRAGMENT LENGTH POLYMORPHISM;

ADOLESCENT; ADULT; AGED; AMINOGLYCOSIDES; CASE-CONTROL STUDIES; CHILD; CHILD, PRESCHOOL; DNA, MITOCHONDRIAL; GENE DELETION; GENE FREQUENCY; GENES, DOMINANT; GENES, RECESSIVE; HEARING; HEARING LOSS, SENSORINEURAL; HUMANS; INFANT; INFANT, NEWBORN; MIDDLE AGED; MUTATION; PEDIGREE; THYMINE;

EID: 19444371441     PISSN: 03858146     EISSN: None     Source Type: Journal    
DOI: 10.1016/j.anl.2005.01.010     Document Type: Article

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