Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.
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C. Nofziger | P. Beck‐Peccoz | M. Paulmichl | L. Fugazzola | E. Salvioni | S. Rodighiero | V. Vezzoli | G. Bottà | G. Meyer | S. Dossena | Elisabeth Grabmayer | M. Boccazzi