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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

Crossref DOI link: https://doi.org/10.1016/j.nrleng.2018.07.007

Published Print: 2020-09

Update policy: https://doi.org/10.1016/elsevier_cm_policy

Authors

Urtiaga Valle, S.

Fournier Gil, B.

Ramiro León, M.S.

Martínez Menéndez, B.
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Article 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

Journal Title: Neurología (English Edition)

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.nrleng.2018.07.007

CrossRef DOI link to the associated document: https://doi.org/10.1016/j.nrl.2018.07.001

Content Type: simple-article

Copyright: © 2018 Sociedad Española de Neurología. Published by Elsevier España, S.L.U.

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