HMN 2025: What is the Genetic trigger for uncommon childhood mind developmental dysfunction
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Credit: The American Journal of Human Genetics (2025). DOI: 10.1016/j.ajhg.2025.05.013 University of Otago–?t?kou Whakaihu Waka…
Recurrent de novo variants in the spliceosomal factor CRNKL1 are associated with severe microcephaly and pontocerebellar hypoplasia with seizures
Overview of attention for article published in American Journal of Human Genetics, June 2025
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