A. López de Munaín Arregui

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease.

M. Gómez Gallego, I. Jericó, J. Díaz-Manera, 2020, Neurologia.

Risk factors associated with COVID-19 infection and mortality in nursing homes

A. López de Munaín Arregui, Alexander Ferro Uriguen, I. B. Telleria, 2022, Atención Primaria.

Patients with a phenotype consistent with facioscapulohumeral muscular dystrophy display genetic and epigenetic heterogeneity

L. Salviati, C. Desnuelle, R. Lemmers, 2011, Journal of Medical Genetics.

Clinical guide for the diagnosis and follow-up of myotonic dystrophy type 1, MD1 or Steinert's disease

M. Gómez Gallego, I. Jericó, J. Díaz-Manera, 2019, Neurología (English Edition).

Inter-individual differences in CpG methylation at D4Z4 correlate with clinical variability in FSHD1 and FSHD2.

Daniel G. Miller, J. Goeman, S. Tapscott, 2015, Human molecular genetics.