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.

Authors

T W Prior¹, C Bartolo, A C Papp, P J Snyder, M S Sedra, A H Burghes, J R Mendell

Affiliation

¹ Department of Pathology, Ohio State University, Columbus 43210.

PMID: 7981690
DOI: 10.1093/hmg/3.7.1173

No abstract available

Publication types

Research Support, Non-U.S. Gov't

MeSH terms

Base Sequence
Dystrophin / genetics*
Exons / genetics*
Genes
Humans
Male
Molecular Sequence Data
Muscular Dystrophies / genetics*
Polymerase Chain Reaction
Polymorphism, Genetic*
Sequence Deletion*

Substances

Dystrophin