Forschung & Innovation
Publikationen
Functional characterization of pendrin mutations found in the Israeli and Palestinian populations.
PMU Autor*innen
Silvia Dossena, Charity Nofziger, Markus Paulmichl
Alle Autor*innen
Silvia Dossena, Charity Nofziger, Zippora Brownstein, Moien Kanaan, Karen B Avraham, Markus Paulmichl
Fachzeitschrift
Cellular physiology and biochemistry
Kurzfassung
Keywords
SYNDROME GENE, WILD-TYPE, INNER-EAR, VESTIBULAR AQUEDUCT, HEARING-LOSS, BICARBONATE SECRETION, IODIDE EFFLUX, GENOTYPE-PHENOTYPE CORRELATION, ENDOPLASMIC-RETICULUM, SLC26A4 GENE