Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.
Article Details
- CitationCopy to clipboard
Prior TW, Bartolo C, Papp AC, Snyder PJ, Sedra MS, Burghes AH, Mendell JR
Identification of a missense mutation, single base deletion and a polymorphism in the dystrophin exon 16.
Hum Mol Genet. 1994 Jul;3(7):1173-4. doi: 10.1093/hmg/3.7.1173.
- PubMed ID
- 7981690 [ View in PubMed]
- Abstract
Not Available