A hereditary spastic paraplegia predominant phenotype caused by variants in the NEFL gene
| Autor: | Mul, Karlien, Schouten, Meyke I., van der Looij, Erica, Dooijes, Dennis, Hennekam, Frederic A.M., Notermans, Nicolette C., Praamstra, Peter, van Gaalen, Judith, Kamsteeg, Erik-Jan, Verbeek, Nienke E., van de Warrenburg, Bart P.C. |
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| Zdroj: | In Parkinsonism and Related Disorders November 2020 80:98-101 |
| Databáze: | ScienceDirect |
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