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, 2003Chicago 2003
Localização: FM - Fac. Medicina (FM BCSEP 2003 253 )(Acessar)
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fm bcsep 2003 293
fm bcsep 2003 032@8
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