Whole-exome sequencing identifies a potential TTN mutation in a multiplex family with inguinal hernia

Por Mihailov, E., Nikopensius, T., Reigo, A., Nikkolo, C., Kals, M., Aruaas, K., Milani, L., Seepter, H., Metspalu, A.
Publicado no Hernia (2016)