Genetic and clinical features of sensorineural hearing loss associated with the 1555 mitochondrial mutation

Laryngoscope

Volumn 107, Issue 4, 1997, Pages 483-490

  Usami, Shin Ichi ^a   Abe, Satoko ^a   Kasai, Miyo ^a   Shinkawa, Hideichi ^a   Moeller, Benjamin ^b   Kenyon, Judy B ^b   Kimberling, William J ^b  

^a HIROSAKI UNIVERSITY   (Japan)

^b BOYS TOWN NATIONAL RESEARCH HOSPITAL   (United States)

Author keywords

[No Author keywords available]

Indexed keywords

AMINOGLYCOSIDE ANTIBIOTIC AGENT;

ADOLESCENT; ADULT; AGED; ANTIBIOTIC THERAPY; ARTICLE; CLINICAL ARTICLE; GENETIC ASSOCIATION; HUMAN; HUMAN CELL; HUMAN TISSUE; JAPAN; MITOCHONDRIAL MYOPATHY; NUCLEOTIDE SEQUENCE; OTOTOXICITY; PEDIGREE; PERCEPTION DEAFNESS; PRIORITY JOURNAL; SCHOOL CHILD;

AMINOGLYCOSIDES; ASIAN CONTINENTAL ANCESTRY GROUP; AUDIOMETRY; GENETIC PREDISPOSITION TO DISEASE; HEARING LOSS, SENSORINEURAL; HUMANS; JAPAN; PEDIGREE; POINT MUTATION; RNA; VESTIBULAR FUNCTION TESTS;

EID: 0031004773     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-199704000-00011     Document Type: Article

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