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

Centre for Neuromuscular and Neurological Disorders (Perron Institute)
UWA Centre for Medical Research (affiliated with the Harry Perkins Institute of Medical Research)

Research output: Contribution to journal › Article › peer-review

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

Cite this

@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 = "American Journal of Medical Genetics Part A",

issn = "0148-7299",

publisher = "Wiley-Liss",

}

TY - JOUR

T1 - Two distinct mutations in a single dystrophin gene: identification of an altered splice-site as the primary Becker muscular dystrophy mutation

AU - Wilton, Steve

AU - Johnson, R.D.

AU - Pedretti, J.R.

AU - Laing, Nigel

PY - 1993

Y1 - 1993

M3 - Article

VL - 46

SP - 563

EP - 569

JO - American Journal of Medical Genetics Part A

JF - American Journal of Medical Genetics Part A

SN - 0148-7299

ER -