Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12530/54432
Title: Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: De novo mutation of the KIF1A gene, a new hope in prognosis
Authors: 
Filiation: Servicio de Neurología, Hospital Universitario de Getafe, Getafe, Madrid, España
Servicio de Genética, Hospital Universitario de Getafe, Getafe, Madrid, España.
Keywords: Paraplegia
Mesh: 
Decs: 
Issue Date: Sep-2020
Publisher: Elsevier
Citation: Urtiaga Valle S, Fournier Gil B, Ramiro León MS, Martínez Menéndez B. Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: De novo mutation of the KIF1A gene, a new hope in prognosis. Neurologia (Engl Ed). 2020 Sep;35(7):535-538. doi: 10.1016/j.nrl.2018.07.001.
PMID: 30862385
URI: https://hdl.handle.net/20.500.12530/54432
Rights: info:eu-repo/semantics/openAccess
CC0 1.0 Universal
ISSN: 2173-5808
Appears in Collections:Hospitales > H. U. de Getafe > Artículos

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