Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder

Clinical Dysmorphology 2026

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Authors: J. S. L. Chan, Stephanie K. L. Ho, Shirley S. W. Cheng, Ho‐Ming Luk

DOI: 10.1097/mcd.0000000000000554

Cited by: 0

Fields of Study & Subjects

Genetics and Neurodevelopmental Disorders Genomics and Rare Diseases Fetal and Pediatric Neurological Disorders