Phenotypes and genotypes in non ‐consanguineous and consanguineous primary microcephaly: High incidence of epilepsy

ConclusionOur findings will help to prioritize genomic investigations, accelerate molecular diagnoses, and improve the management of PM patients.

Source: Molecular Genetics & Genomic Medicine - August 17, 2021 Category: Genetics & Stem Cells Authors: Sarah Duerinckx, Julie D ésir, Camille Perazzolo, Cindy Badoer, Valérie Jacquemin, Julie Soblet, Isabelle Maystadt, Yusuf Tunca, Bettina Blaumeiser, Berten Ceulemans, Winnie Courtens, François‐Guillaume Debray, Anne Destree, Koenraad Dev Tags: ORIGINAL ARTICLE Source Type: research