Judit García

Mutations affecting mRNA splicing are the most common molecular defects in patients with neurofibromatosis type 1.

X. Estivill, C. Lázaro, E. Ars, 2000, Human molecular genetics.

CD98hc (SLC3A2) sustains amino acid and nucleotide availability for cell cycle progression

Z. Ignatova, M. Palacín, J. Chillarón, 2019, Scientific Reports.