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Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype.

Document Type

Article

Author

Wafik, Mohamed; Kuoppamaa, Heidi; Hirani, Priyal; Hignett, John; Lillis, Suzanne; Lascelles, Karine; Sardesai, Shweta; Gomez, Kumudini; Holder-Espinasse, Muriel

Source

Clinical Dysmorphology; Jul2023, Vol. 32 Issue 3, p116-123, 8p

Subject

Language

ISSN

09628827

Online Access

Full Text (LWW Journals - Ovid) Full Text (LWW total - Ovid) Web of Science JCR 저널정보 Scopus Find it@PNU

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