Two novel CSNK2A1 variants associated with mild Okur-Chung neurodevelopmental syndrome phenotype : Clinical Dysmorphology

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

Wafik, Mohameda; Kuoppamaa, Heidib; Hirani, Priyalb; Hignett, Johnb; Lillis, Suzanneb; Lascelles, Karinec; Sardesai, Shwetad; Gomez, Kumudinie; Holder-Espinasse, Muriela

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Clinical Dysmorphology 32(3):p 116-123, July 2023. | DOI: 10.1097/MCD.0000000000000456
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