Mice, Inbred mdx
A strain of mice arising from a spontaneous MUTATION (mdx) in inbred C57BL mice. This mutation is X chromosome-linked and produces viable homozygous animals that lack the muscle protein DYSTROPHIN, have high serum levels of muscle ENZYMES, and possess histological lesions similar to human MUSCULAR DYSTROPHY. The histological features, linkage, and map position of mdx make these mice a worthy animal model of DUCHENNE MUSCULAR DYSTROPHY.
Year introduced: 1994
PubMed search builder options
Subheadings:
Tree Number(s): B01.050.050.199.520.520.420.500, B01.050.150.900.649.313.992.635.505.500.400.420.500, B01.050.150.900.649.313.992.635.505.500.550.265
MeSH Unique ID: D018101
Entry Terms:
- Inbred mdx Mice
- Mice, mdx
- mdx Mice
- Mouse, mdx
- mdx Mouse
- Mouse, Inbred mdx
- Inbred mdx Mouse
Previous Indexing:
See Also: