ArticleMolecular genetics & genomic medicine2026
Correction to "A Case of CSNK2A1 Gene Variant Causing Okur-Chung Syndrome and Analysis of the Clinical Phenotypic Spectrum".
PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.
ArticleMolecular genetics & genomic medicine2026
PubMed ↗Full text ↗Publisher ↗
No numbers read from the abstract.