Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48-Reference-Cited by-同舟云学术

Overlapping phenotypes in complex spastic paraplegias SPG11, SPG15, SPG35 and SPG48

Published:2014-05-15 Issue:7 Volume:137 Page:1907-1920
ISSN:1460-2156
Container-title:Brain
language:en
Short-container-title:

Author:

Pensato Viviana,Castellotti Barbara,Gellera Cinzia,Pareyson Davide,Ciano Claudia,Nanetti Lorenzo,Salsano Ettore,Piscosquito Giuseppe,Sarto Elisa,Eoli Marica,Moroni Isabella,Soliveri Paola,Lamperti Elena,Chiapparini Luisa,Di Bella Daniela,Taroni Franco,Mariotti Caterina

Publisher

Oxford University Press (OUP)

Subject

Clinical Neurology

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5. A rare family with Hereditary Spastic Paraplegia Type 35 due to novel FA2H mutations: a case report with literature review;Cao;J Neurol Sci,2013

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