https://repositorio.una.ac.cr/items/c1cb940a-bc7c-4f2e-8602-6d1b10ebb04d
Identification of the variant Ala335Val of MED25 as responsible for CMT2B2: molecular data,...
Charcot-Marie-Tooth (CMT) disease is a clinically and genetically heterogeneous disorder. All mendelian patterns of inheritance have been described. We...
of the