New molecular mechanism for ullrich congenital muscular dystrophy a heterozygous in-frame deletion in the COL6A1 gene causes a severe phenotype
Te-Cheng Pan Rui Zhu Zhang; Dominick G Sudano; Suely K Marie; Carsten G Bonnemann; Mon Li Chu
American Journal of Human Genetics Chicago v. 73, p. 355-369, 2003
Chicago 2003
Localização:
FM - Fac. Medicina
(FM BCSEP 2003 253 )(Acessar)