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Case Reports in Neurological Medicine
Volume 2019, Article ID 7615605, 5 pages
Case Report

CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76

1Tecnologico de Monterrey, Escuela de Medicina y Ciencias de la Salud, Monterrey, Nuevo Leon, Mexico
2Department of Neurology, Christian-Albrechts University, Kiel, Germany

Correspondence should be addressed to Daniel Martinez-Ramirez; xm.dulascet.socidem@zenitram.leinad

Received 3 May 2019; Accepted 23 May 2019; Published 1 July 2019

Academic Editor: Federico Micheli

Copyright © 2019 Jesus Eduardo Garcia-Berlanga et al. This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

How to Cite this Article

Jesus Eduardo Garcia-Berlanga, Mariana Moscovich, Isaac Jair Palacios, Alejandro Banegas-Lagos, Augusto Rojas-Martinez, and Daniel Martinez-Ramirez, “CAPN1 Variants as Cause of Hereditary Spastic Paraplegia Type 76,” Case Reports in Neurological Medicine, vol. 2019, Article ID 7615605, 5 pages, 2019.