Article
Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype.
Clinical dysmorphology - 1 Jul 2023
Wafik Mohamed, Kuoppamaa Heidi, Hirani Priyal, Hignett John, Lillis Suzanne, Lascelles Karine, Sardesai Shweta, Gomez Kumudini, Holder-Espinasse Muriel
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