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Studying Rare Movement Disorders: From Whole-Exome Sequencing to New Diagnostic and Therapeutic Approaches in a Modern Genetic Clinic by Luca Marsili, Kevin R. Duque, Jesus Abanto, Nathaly O. Chinchihualpa Paredes, Andrew P. Duker, Kathleen Collins, Marcelo Miranda, M. Leonor Bustamante, Michael Pauciulo, Michael Dixon, Hassan Chaib, Josefina Perez-Maturo, Emily J. Hill, Alberto J. Espay, Marcelo A. Kauffman
Published 2024-11-01Get full text
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Whole genome sequencing reveals a de novo SHANK3 mutation in familial autism spectrum disorder. by Sergio I Nemirovsky, Marta Córdoba, Jonathan J Zaiat, Sabrina P Completa, Patricia A Vega, Dolores González-Morón, Nancy M Medina, Mónica Fabbro, Soledad Romero, Bianca Brun, Santiago Revale, María Florencia Ogara, Adali Pecci, Marcelo Marti, Martin Vazquez, Adrián Turjanski, Marcelo A Kauffman
Published 2015-01-01Get full text
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