Variable penetrance of COL6A1 null mutations: Implications for prenatal diagnosis and genetic counselling in Ullrich congenital muscular dystrophy families
Rachel A. Peat, Naomi L. Baker, Kristi J. Jones, Kathryn N. North, Shireen R. LamandéVolume:
17
Year:
2007
Language:
english
DOI:
10.1016/j.nmd.2007.03.017
File:
PDF, 1.16 MB
english, 2007