Mutations of the Pendred syndrome gene (PDS) in patients with large vestibular aqueduct

Acta Oto-Laryngologica

Volumn 120, Issue 2, 2000, Pages 137-141

  Kitamura, Ken ^a,d   Takahashi, Katsumasa ^b   Noguchi, Yoshihiro ^a   Kuroishikawa, Yasushi ^a   Tamagawa, Yuya ^b   Ishikawa, Kotaro ^b   Ichimura, Keiichi ^b   Hagiwara, Hideo ^c  

^a TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

^b JICHI MEDICAL UNIVERSITY   (Japan)

^c Nanae Clinic   (Japan)

^d TOKYO MEDICAL AND DENTAL UNIVERSITY   (Japan)

Author keywords

Hearing loss fluctuation; Missense mutation; Vertigo

Indexed keywords

CARRIER PROTEIN; SLC26A4 PROTEIN, HUMAN;

ADOLESCENT; ADULT; ARTICLE; CHILD; COMPUTER ASSISTED TOMOGRAPHY; CONGENITAL MALFORMATION; FEMALE; GENETICS; GOITER; HUMAN; MALE; NUCLEAR MAGNETIC RESONANCE IMAGING; NUCLEOTIDE SEQUENCE; PATHOLOGY; PERCEPTION DEAFNESS; PURE TONE AUDIOMETRY; SYNDROME; VESTIBULE AQUEDUCT;

ADOLESCENT; ADULT; AUDIOMETRY, PURE-TONE; CARRIER PROTEINS; CHILD; DNA MUTATIONAL ANALYSIS; FEMALE; GOITER; HEARING LOSS, SENSORINEURAL; HUMANS; MAGNETIC RESONANCE IMAGING; MALE; MEMBRANE TRANSPORT PROTEINS; SYNDROME; TOMOGRAPHY, X-RAY COMPUTED; VESTIBULAR AQUEDUCT;

EID: 0034157691     PISSN: 00016489     EISSN: None     Source Type: Journal    
DOI: 10.1080/000164800750000775     Document Type: Article

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