Elisabeth Grabmayer

发表

Molecular and Functional Characterization of Human Pendrin and its Allelic Variants

C. Nofziger, G. Tamma, M. Paulmichl, 2011, Cellular Physiology and Biochemistry.

Functional characterization of wild-type and mutated pendrin (SLC26A4), the anion transporter involved in Pendred syndrome.

C. Nofziger, P. Beck‐Peccoz, M. Paulmichl, 2009, Journal of molecular endocrinology.