RET haplotype, not linked to the C620R activating mutation, associated with Hirschsprung disease in a novel MEN2 family. Clinics, [S. l.], v. 67, n. supl.1, p. 57–61, 2012. DOI: 10.6061/clinics/2012(Sup01)11. Disponível em: https://www.revistas.usp.br/clinics/article/view/19722.. Acesso em: 15 may. 2024.