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Neurology perspectives MAPT gene mutation in familiar progressive supranuclear palsy, a case report
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MAPT gene mutation in familiar progressive supranuclear palsy, a case report
Mutación del gen MAPT en la parálisis supranuclear progresiva familiar, reporte de un caso
M. Rodrígueza,
Corresponding author
jmrodriguezl@unbosque.edu.co

Corresponding author.
, H. Kreinterb, N. Zapaa, O. Oliverosa, C. Jiméneza
a Hospital Simón Bolívar, Neurology Department, Bogotá, Colombia
b Hospital Simón Bolívar, Neurology Resident, Bogotá, Colombia
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ISSN: 26670496
Original language: English
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