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Medicine

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

Joshua C K Chan, S. K. L. Ho, S. Cheng, Ho-Ming Luk

2026.2.9CLINICAL DYSMORPHOLOGY

DOI: 10.1097/mcd.0000000000000554

Abstract

Abstract is not available.

Citation format

CHAN, Joshua C K, et al. Additional case report supports loss-of-function CCNK variants being causative for a recognizable syndromic neurodevelopmental disorder. CLINICAL DYSMORPHOLOGY, 2026, 35(2): 74–76.