IRF2BPL gene variants with dystonia: one new Chinese case report
Abstract Background The carriers of damaging heterozygous variants in interferon regulatory factor 2 binding protein-like (IRF2BPL), encoding a member of the IRF2BP family of transcriptional regulators, may be affected by a variety of neurological symptoms, such as neurodevelopmental regression, lan...
| Egile Nagusiak: | , , , , |
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| Formatua: | Artikulua |
| Hizkuntza: | English |
| Argitaratua: |
BMC
2023-01-01
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| Saila: | BMC Neurology |
| Gaiak: | |
| Sarrera elektronikoa: | https://doi.org/10.1186/s12883-023-03077-x |