V. Milić-Rašić

Targeted next-generation sequencing of a 12.5 Mb homozygous region reveals ANO10 mutations in patients with autosomal-recessive cerebellar ataxia.

A. Hoischen, N. Drouot, J. Veltman, 2010, American journal of human genetics.

Glucose and lipid metabolism disorders in children and adolescents with spinal muscular atrophy types 2 and 3

V. Milic-Rasic, L. Marković-Denić, V. Zdravkovic, 2021, Neuromuscular Disorders.

Cardiac findings in pediatric patients with spinal muscular atrophy types 2 and 3

G. Vukomanovic, V. Milic-Rasic, L. Marković-Denić, 2020, Muscle & nerve.

Further developments with antisense treatment for myasthenia gravis

H. Soreq, Z. Argov, J. Sussman, 2012, Annals of the New York Academy of Sciences.