A mild and unusual CMT compound phenotype due to the presence of two mutations in pmP22 gene 17p duplication and Ser72Leuc
Wilson Marques Júnior Silmara S. P. G Lima; Vinicius H. S Borghtti; Keity C Bueno; Amilton Antunes Barreira; Annual Meeting of The American Academy of Neurology (60. 2008 Chicago)
Neurology Philadelphia v. 70, n. 11, suppl. 1, p. A313, res. P06.058, 2008Philadelphia 2008
Localização: FMRP - Fac. Medicina de Ribeirão Preto (pcd 1669388 ) e outros locais(Acessar)