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Literature for DOID 0080918: polymicrogyria
Xenbase Articles

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Functional characterization of a novel TP53RK mutation identified in a family with Galloway-Mowat syndrome.,
Treimer E,Kalayci T,Schumann S,Suer I,Greco S,Schanze D,Schmeisser MJ,Kühl SJ,Zenker M,
Hum Mutat. December 1, 2022; 43(12):1098-1004.
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