Wilton S.D.,1993


Wilton S.D., Johnsen R.D., Pedretti J.R., Laing N.G. Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation. - Am.J.Med.Genet., 1993, v. 46, p. 563-569.

Смотрите также:

  • Табл. DMD sp