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Expanding SPG18 clinical spectrum: autosomal dominant mutation causes complicated hereditary spastic paraplegia in a large family

Document Type

Article

Author

Trinchillo, A.; Iovino, A.; Cuomo, N.; Caccavale, C.; Nocerino, C.; Criscuolo, C.; Valente, V.; Picciocchi, M.; De Rosa, L.; Pierantoni, G.M.; Paladino, S.; Esposito, M.; Migliaccio, M.; Salvatore, E.; Menchise, V.

Source

In: Neurological Sciences. (Neurological Sciences, September 2024, 45(9):4373-4381)

Subject

Language

English

ISSN

15903478
15901874

Online Access

Web of Science JCR 저널정보 Scopus Find it@PNU

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