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Autor:
J T, Den Dunnen, P M, Grootscholten, E, Bakker, L A, Blonden, H B, Ginjaar, M C, Wapenaar, H M, van Paassen, C, van Broeckhoven, P L, Pearson, G J, van Ommen
Publikováno v:
American journal of human genetics. 45(6)
We have studied 34 Becker and 160 Duchenne muscular dystrophy (DMD) patients with the dystrophin cDNA, using conventional blots and FIGE analysis. One hundred twenty-eight mutations (65%) were found, 115 deletions and 13 duplications, of which 106 de