A Case of Okur-Chung Neurodevelopmental Syndrome with a Novel, de novo Variant on the CSNK2A1 Gene in a Turkish Patient.
| Autor: | Zhuri, Drenushe, Dusenkalkan, Fulya, Tunca Alparslan, Guzin, Gurkan, Hakan |
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| Zdroj: | Molecular Syndromology; 2024, Vol. 15 Issue 1, p43-50, 8p |
| Databáze: | Complementary Index |
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