Treimer, E. Et Al. 2022. Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome. HUMAN MUTATION , vol.43, no.12 , 1866-1871.

Treimer, E., Kalayci, T., Schumann, S., Suer, I., Greco, S., Schanze, D., ... Schmeisser, M. J.(2022). Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome. HUMAN MUTATION , vol.43, no.12, 1866-1871.

Treimer, Ernestine Et Al. "Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome," HUMAN MUTATION , vol.43, no.12, 1866-1871, 2022

Treimer, Ernestine Et Al. "Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome." HUMAN MUTATION , vol.43, no.12, pp.1866-1871, 2022

Treimer, E. Et Al. (2022) . "Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome." HUMAN MUTATION , vol.43, no.12, pp.1866-1871.

@article{article, author={Ernestine Treimer Et Al. }, title={Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome}, journal={HUMAN MUTATION}, year=2022, pages={1866-1871} }