Novel phenotype with prominent cerebellar oculomotor dysfunction in spastic paraplegia type 39

OBJECTIVES: The term hereditary spastic paraplegia comprises an ever-expanding array of neurological disorders with distinct aetiologies. Spastic paraplegia gene 39 is one of the many genetically defined types with features of other organs and neurological systems in addition to paraspasticity. We d...

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Detalles Bibliográficos
Autores principales: Viertauer, Sebastian, Kurth, Ingo, Eggermann, Katja, Eggers, Christian
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2022
Materias:
Original Communication
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618546/
https://www.ncbi.nlm.nih.gov/pubmed/35947152
http://dx.doi.org/10.1007/s00415-022-11313-6

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618546/
https://www.ncbi.nlm.nih.gov/pubmed/35947152
http://dx.doi.org/10.1007/s00415-022-11313-6

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