Integration of human and mouse genetics reveals pendrin function in hearing and deafness

Cellular Physiology and Biochemistry

Volumn 28, Issue 3, 2011, Pages 535-544

  Dror, Amiel A ^a   Brownstein, Zippora ^a   Avraham, Karen B ^a  

^a TEL AVIV UNIVERSITY   (Israel)

Author keywords

Enlarged vestibular aqueduct; Hearing loss; Massively parallel sequencing; Otoconia; SLC26A4

Indexed keywords

CALCIUM CARBONATE; CALCIUM OXALATE; PENDRIN;

ANIMAL EXPERIMENT; ANIMAL MODEL; ANIMAL TISSUE; COCHLEA; GENE MUTATION; GENOTYPE PHENOTYPE CORRELATION; HEARING LOSS; HUMAN; MORPHOLOGY; MOUSE; NONHUMAN; OTOLITH; PENDRED SYNDROME; PRIORITY JOURNAL; REVIEW; SACCULUS; SCANNING ELECTRON MICROSCOPY; UTRICLE; VESTIBULE AQUEDUCT;

EID: 82255167107     PISSN: 10158987     EISSN: 14219778     Source Type: Journal    
DOI: 10.1159/000335163     Document Type: Review

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