Functional characterization of pendrin mutations found in the Israeli and Palestinian populations

Cellular Physiology and Biochemistry

Volumn 28, Issue 3, 2011, Pages 477-484

  Dossena, Silvia ^a   Nofziger, Charity ^a   Brownstein, Zippora ^b   Kanaan, Moien ^c   Avraham, Karen B ^b   Paulmichl, Markus ^a  

^a PARACELSUS MEDICAL UNIVERSITY   (Austria)

^b TEL AVIV UNIVERSITY   (Israel)

^c BETHLEHEM UNIVERSITY   (Israel)

Author keywords

EVA; Functional test; Inherited hearing loss; Ion transport; Pendred syndrome; Pendrin; SLC26A4

Indexed keywords

COMPLEMENTARY DNA; HALIDE; PENDRIN; PLASMID DNA;

ALLELE; ARTICLE; AUTOSOMAL RECESSIVE DISORDER; CELL PH; CELL STRAIN HEK293; CONTROLLED STUDY; ETHNIC GROUP; GENE MUTATION; HEARING LOSS; HUMAN; HUMAN CELL; INNER EAR; ION TRANSPORT; ISRAEL; MAJOR CLINICAL STUDY; PALESTINE; PENDRED SYNDROME; POPULATION GENETICS; PRIORITY JOURNAL; VESTIBULE AQUEDUCT;

EID: 82255196439     PISSN: 10158987     EISSN: 14219778     Source Type: Journal    
DOI: 10.1159/000335109     Document Type: Article

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