Bilateral sensorineural hearing loss associated with the point mutation in mitochondrial genome

Laryngoscope

Volumn 106, Issue 1 I, 1996, Pages 43-48

  Oshima, Takeshi ^a   Ueda, Narihisa ^a   Ikeda, Katsuhisa ^a   Abe, Koji ^a   Takasaka, Tomonori ^a  

^a TOHOKU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

Author keywords

[No Author keywords available]

Indexed keywords

MITOCHONDRIAL DNA;

ADOLESCENT; ADULT; AGED; ARTICLE; AUDIOGRAPHY; AUDITORY NERVOUS SYSTEM; CLINICAL ARTICLE; CLINICAL FEATURE; COCHLEA; DIABETES MELLITUS; FEMALE; GENETIC ANALYSIS; HUMAN; HUMAN CELL; MALE; MELAS SYNDROME; MITOCHONDRION; MUTATION; PERCEPTION DEAFNESS; POINT MUTATION; POLYMERASE CHAIN REACTION; PRIORITY JOURNAL;

ADOLESCENT; ADULT; AMINO ACID SEQUENCE; COCHLEA; DIABETES MELLITUS, TYPE 2; DNA, MITOCHONDRIAL; FEMALE; GENOME; HEARING LOSS, BILATERAL; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; MOLECULAR SEQUENCE DATA; POINT MUTATION;

EID: 0030059395     PISSN: 0023852X     EISSN: None     Source Type: Journal    
DOI: 10.1097/00005537-199601000-00009     Document Type: Article

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