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Letter to the Editor
Usefulness of exome sequencing in the study of spastic paraparesis and cerebellar atrophy: de novo mutation of the KIF1A gene, a new hope in prognosis
Utilidad del exoma en el estudio de la paraparesia espástica y la atrofia cerebelosa: mutación de novo en el gen KIF1A, una nueva esperanza pronóstica
S. Urtiaga Vallea,
Corresponding author
sarai.urtiaga@gmail.com

Corresponding author.
, B. Fournier Gilb, M.S. Ramiro Leónb, B. Martínez Menéndeza
a Servicio de Neurología, Hospital Universitario de Getafe, Getafe, Madrid, Spain
b Servicio de Genética, Hospital Universitario de Getafe, Getafe, Madrid, Spain
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ISSN: 21735808
Original language: English
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