Rare diseases, despite their individual rarity, collectively affect millions worldwide, posing significant challenges to diagnosis, treatment, and understanding. Genomics and bioinformatics play crucial roles in unravelling the genetic underpinnings of these diseases, aiding in the identification of causative mutations, elucidation of disease mechanisms, and development of targeted therapies.
G&I invites researchers and experts in the field to contribute their latest findings and insights to this collection entitled 'Frontiers in Rare Disease Genetics,' edited by Dr. Murim Choi, vice-editor-in-chief. We encourage submissions that push the boundaries of knowledge in rare disease genetics.
To facilitate the dissemination of impactful research, selected articles may have their publication fees covered by the Korea Genome Organization (KOGO).
Join us in advancing rare disease research and fostering collaboration within the scientific community!