Letter to the Editor
A Spanish family with a compound heterozygous mutation in SPG7: From uncertainty to clinical reality
Familia española portadora de una mutación en heterocigosis compuesta en el gen SPG7: de la incertidumbre a la realidad clínica
M.C. Fernández-Morenoa,
, C. Castro-Fernándezb, M.M. Viloria-Peñasc, L. Castilla-Guerrad
Corresponding author
a Servicio de Neurología, Hospital Universitario Virgen de Valme, Universidad de Sevilla, Sevilla, Spain
b Grupo Neurogenetica, Instituto de Investigación Sanitaria de Santiago de Compostela (IDIS), Santiago de Compostela, La Coruña, Spain
c Servicio de Bioquímica Clínica, Hospital Universitario Virgen de Valme, Sevilla, Spain
d Servicio de Medicina Interna, Hospital Universitario Virgen Macarena, Universidad de Sevilla, Sevilla, Spain
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