Article
A Novel Compound Heterozygous Genotype of the WDR73 Gene Associated With a Psychomotor Retardation Syndrome Without Cerebellar Atrophy and Other CNS Structural Abnormalities.
Clinical genetics - 1 Feb 2025
Nogueira Enrique, Del Olmo Beatriz, Babín Lara, Vizuete Génesis, Lobo Concepción, González Cecilia
Abstract excerpt
A novel compound heterozygous genotype of the WDR73 gene associated with a psychomotor retardation syndrome without cerebellar atrophy and other CNS structural abnormalities.
Read the complete abstract on PubMedTopics
Share this publication in a Topic to start or enrich a Post.