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Next generation sequencing for rapid diagnosis of a rare early onset spastic paraplegia: A novel pathological variant in FA2H gene

Crossref DOI link: https://doi.org/10.1016/j.labcli.2018.01.004

Published Print: 2018-10

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

Authors

González-González, M. Cristina

Gutierrez, Miriam

de la Mota, Cristina Castaño

Jareño, Nuria Muñoz

Gonzalez, Severino

Cava, Fernando
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Article Title: Next generation sequencing for rapid diagnosis of a rare early onset spastic paraplegia: A novel pathological variant in FA2H gene

Journal Title: Revista del Laboratorio Clínico

CrossRef DOI link to publisher maintained version: https://doi.org/10.1016/j.labcli.2018.01.004

Content Type: simple-article

Copyright: © 2018 AEBM, AEFA y SEQC. Published by Elsevier España, S.L.U. All rights reserved.