Casuística
Nueva mutación en SPG11 en una paciente con paraplejía espástica hereditaria complicada: hallazgos clínicos-electrofisiológicos y moleculares
Novel mutation in SPG11 in a patient with hereditary spastic paraplegia: Clinical, electrophysiological and molecular findings
Andrés Berardoa,b,
, Lucía Schottlaenderc, Ramón Leiguardad, Henry Houldenc, Ricardo Reisine
Autor para correspondencia
a Servicio de Neurología, Hospital Universitario Austral (HUA), Buenos Aires, Argentina
b Instituto de Neurociencias Conci Carpinella, Córdoba Argentina
c Department of Molecular Neuroscience, Institute of Neurology, UCL, Londres, Reino Unido
d Servicio de Neurología, Instituto FLENI, Buenos Aires, Argentina
e Servicio de Neurología, Hospital Británico, Buenos Aires, Argentina
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