Hereditary sensorineural hearing loss of unknown cause involving mitachondrial DNA 1555 mutation

ORL

Volumn 62, Issue 2, 2000, Pages 100-103

  Iwasaki, Satoshi ^a   Tamagawa, Yuya ^b   Ocho, Shuji ^a   Hoshino, Tomoyuki ^a   Kitamura, Ken ^b  

^a HAMAMATSU UNIVERSITY SCHOOL OF MEDICINE   (Japan)

^b JICHI MEDICAL UNIVERSITY   (Japan)

Author keywords

1555 point mutation; Aminoglycoside; Mitochondrial DNA; Sensorineural hearing loss

Indexed keywords

AMINOGLYCOSIDE; MITOCHONDRIAL DNA;

ADULT; ARTICLE; CASE REPORT; EXTRACHROMOSOMAL INHERITANCE; HUMAN; MALE; MOTHER; NUCLEIC ACID BASE SUBSTITUTION; PERCEPTION DEAFNESS; POINT MUTATION; PRIORITY JOURNAL; SIBLING;

EID: 0034093499     PISSN: 03011569     EISSN: None     Source Type: Journal    
DOI: 10.1159/000027725     Document Type: Article

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