Rare genetic causes of primary microcephaly in two Saudi families identified via whole-exome sequencing: Genomic and phenotypic delineation of pathogenic CDK5RAP2 and CIT variants
Authors: Daniah Albokhari, Rayya Almarwani, Emad Khadawardi et al.
Publication: Molecular Genetics and Metabolism Reports
Published: Jun 1, 2026
Source: Crossref