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Case Report: Long-Term Treatment and Follow-Up of Kleefstra Syndrome-2
BACKGROUND: Mutations in the KMT2C gene can cause Kleefstra syndrome-2 (KLEFS2). CASE: In this study, we analyzed the clinical, genetic testing, and 10-year follow-up data of a child with KLEFS2 treated at the Child Healthcare Department, Children's Hospital of Nanjing Medical University, Nanji...
| Autores principales: | , |
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| Formato: | Online Artículo Texto |
| Lenguaje: | English |
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Frontiers Media S.A.
2022
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| Materias: | |
| Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9172761/ https://www.ncbi.nlm.nih.gov/pubmed/35685914 http://dx.doi.org/10.3389/fped.2022.881838 |