Abstract
We have identified a novel T-insertion polymorphism located in the second intron of the dystrophin gene. This polymorphism should prove useful in linkage studies in Duchenne and Becker muscular dystrophy families in addition to the previously described markers.
Publication types
-
Research Support, Non-U.S. Gov't
MeSH terms
-
DNA Transposable Elements*
-
Dystrophin / genetics*
-
Gene Frequency
-
Humans
-
Introns
-
Muscular Dystrophies / genetics*
-
Polymerase Chain Reaction
-
Polymorphism, Genetic*
-
X Chromosome*
Substances
-
DNA Transposable Elements
-
Dystrophin
Associated data
-
GENBANK/L13238
-
GENBANK/L13296
-
GENBANK/L13297
-
GENBANK/L14001
-
GENBANK/L14002
-
GENBANK/L14003
-
GENBANK/X65231
-
GENBANK/X65232
-
GENBANK/X65233
-
GENBANK/X65363