Cite
HARVARD Citation
Treimer, E. et al. (2022). Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome. Human mutation. 43 (12), pp. 1866-1871. [Online].
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Treimer, E. et al. (2022). Functional characterization of a novel TP53RK mutation identified in a family with Galloway–Mowat syndrome. Human mutation. 43 (12), pp. 1866-1871. [Online].