Overwhelming genetic heterogeneity and exhausting molecular diagnostic process in chronic and progressive ataxias: facing it up with an algorithm, a gene, a panel at a time von Perez Maturo, J, Zavala, L, Vega, P, González-Morón, D, Medina, N, Salinas, V, Rosales, J, Córdoba, M, Arakaki, T, Garretto, N, Rodríguez-Quiroga, S, Kauffman, M A

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POLIMORFISMOS SEROTONINÉRGICOS: DISTRIBUCIÓN DE FRECUENCIAS ALÉLICAS Y GENOTÍPICAS EN LA POBLACIÓN DE MAR DEL PLATA, ARGENTINA Y COMPARACIÓN DE MÉTODOS DE GENOTIPADO von Perez, Maturo J, Videla, Y, Di Gerónimo, V, Quintana, S

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EXPANSIÓN FENOTÍPICA DE SCN2A: UTILIDAD DIAGNÓSTICA DE LA SECUENCIACIÓN GENÓMICA von Medina, NM, Maturo, J Perez, Quiroga, SA Rodriguez, Denzler, IM, Moron, D Gonzalez, Kauffman, MA, Vega, PA

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Studying Rare Movement Disorders: From Whole-Exome Sequencing to New Diagnostic and Therapeutic Approaches in a Modern Genetic Clinic von Marsili, Luca, Duque, Kevin R, Abanto, Jesus, Chinchihualpa Paredes, Nathaly O, Duker, Andrew P, Collins, Kathleen, Miranda, Marcelo, Bustamante, M. Leonor, Pauciulo, Michael, Dixon, Michael, Chaib, Hassan, Perez-Maturo, Josefina, Hill, Emily J, Espay, Alberto J, Kauffman, Marcelo A

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Expected Present and Final Value of an Annuity when some Non-Central Moments of the Capitalization Factor are Unknown: Theory and an Application using R von Cruz Rambaud, Salvador, Maturo, Fabrizio, Sánchez Pérez, Ana María

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