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Identification of two point mutations and a one base deletion in exon 19 of the dystrophin gene by heteroduplex formation
Prior, Thomas W., Papp, Audrey C., Snyder, Pamela J., Burghes, Arthur H.M., Sedra, Mary S., Western, Lorraine M., Bartello, Claire, Mendell, Jerry R.Volume:
2
Year:
1993
Language:
english
Journal:
Human Molecular Genetics
DOI:
10.1093/hmg/2.3.311
File:
PDF, 2.00 MB
english, 1993