Nadia M. Murillo-Melo

Dp71 Point Mutations Induce Protein Aggregation, Loss of Nuclear Lamina Integrity and Impaired Braf35 and Ibraf Function in Neuronal Cells

R. Suárez-Sánchez, O. Hernández-Hernández, B. Cisneros, 2022, International journal of molecular sciences.

Origin of the myotonic dystrophy type 1 mutation in Mexican population and influence of Amerindian ancestry on CTG repeat allelic distribution

O. Hernández-Hernández, E. Mendoza-Caamal, Y. Tapia-Guerrero, 2017, Neuromuscular Disorders.

Oropharyngeal dysphagia in early stages of myotonic dystrophy type 1

B. Cisneros, H. Cortés, J. Magaña, 2019, Muscle & nerve.

The Need for Establishing a Universal CTG Sizing Method in Myotonic Dystrophy Type 1

A. Lucia, G. Nogales-Gadea, G. Pintos-Morell, 2020, Genes.