Progressive sensorineural hearing impairment in maternally inherited diabetes mellitus and deafness (MIDD)

Otology and Neurotology

Volumn 27, Issue 6, 2006, Pages 802-808

  Hendrickx, Jan Jaap ^a   Mudde, Aart H ^b   'T Hart, Leen M ^c   Huygen, Patrick L M ^a   Cremers, Cor W R J ^a  

^a RADBOUD UNIVERSITY MEDICAL CENTER   (Netherlands)

^b SLINGELAND HOSPITAL   (Netherlands)

^c LEIDEN UNIVERSITY MEDICAL CENTER   (Netherlands)

Author keywords

Genetic deafness; Human; Mitochondrial genetics; Phenotype; Point mutation; Sensorineural hearing loss

Indexed keywords

ADENINE; GUANINE; MITOCHONDRIAL RNA; TRANSFER RNA;

ADULT; AGED; AMINO ACID SUBSTITUTION; ANAMNESIS; ARTICLE; AUDIOLOGY; AUDITORY THRESHOLD SHIFT; CLINICAL ARTICLE; CLINICAL FEATURE; DISEASE COURSE; EVOKED BRAIN STEM AUDITORY RESPONSE; EVOKED BRAIN STEM RESPONSE; FEMALE; GENE LOCATION; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HEARING; HEARING ACUITY; HEARING IMPAIRMENT; HETEROPLASMY; HUMAN; LEUKOCYTE; MALE; MATERNALLY INHERITED DIABETES AND DEAFNESS; MITOCHONDRIAL GENETICS; MUTATIONAL ANALYSIS; NEUROLOGIC EXAMINATION; PERCEPTION DEAFNESS; PRESBYACUSIS; PRIORITY JOURNAL; PURE TONE AUDIOMETRY; RETROSPECTIVE STUDY; SPEECH AUDIOMETRY; SPEECH DISCRIMINATION; VESTIBULAR TEST;

ADULT; AGED; AUDIOMETRY, EVOKED RESPONSE; AUDIOMETRY, PURE-TONE; DEAFNESS; DIABETES MELLITUS; DIABETES MELLITUS, TYPE 1; DIABETES MELLITUS, TYPE 2; DISEASE PROGRESSION; DNA, MITOCHONDRIAL; FEMALE; GENOTYPE; HEARING LOSS, SENSORINEURAL; HUMANS; MALE; MIDDLE AGED; PHENOTYPE; POINT MUTATION; REGRESSION ANALYSIS; RETROSPECTIVE STUDIES; RNA, TRANSFER, LEU; SEX FACTORS;

EID: 33748309301     PISSN: 15317129     EISSN: 15374505     Source Type: Journal    
DOI: 10.1097/01.mao.0000224091.02506.a0     Document Type: Article

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