Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation

Steve Wilton; R.D. Johnson; J.R. Pedretti; Nigel Laing

Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation

Steve Wilton, R.D. Johnson, J.R. Pedretti, Nigel Laing

Research output: Contribution to journal › Article

Original language	English
Pages (from-to)	563-569
Journal	American Journal of Medical Genetics Part A
Volume	46
Publication status	Published - 1993

Cite this

Wilton, S., Johnson, R. D., Pedretti, J. R., & Laing, N. (1993). Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation. American Journal of Medical Genetics Part A, 46, 563-569.

@article{b271d959e88e46bd88bf9375a126b846,

title = "Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation",

author = "Steve Wilton and R.D. Johnson and J.R. Pedretti and Nigel Laing",

year = "1993",

language = "English",

volume = "46",

pages = "563--569",

journal = "Am J Med Genet A",

issn = "0148-7299",

publisher = "Wiley-Liss",

}