A comparison of the bone and growth phenotype of mdx, mdx:Cmah−/− and mdx:Utrn+/− murine models with the C57BL/10 wild-type mouse

The muscular dystrophy X-linked (mdx) mouse is commonly used as a mouse model of Duchenne muscular dystrophy (DMD). Its phenotype is, however, mild, and other mouse models have been explored. The mdx:Cmah−/− mouse carries a human-like mutation in the Cmah gene and has a severe muscle phenotype, but...

Full description

Saved in:
Bibliographic Details
Main Authors: Claire L. Wood (Author), Karla J. Suchacki (Author), Rob van 't Hof (Author), Will P. Cawthorn (Author), Scott Dillon (Author), Volker Straub (Author), Sze Choong Wong (Author), Syed F. Ahmed (Author), Colin Farquharson (Author), Annemieke Aartsma-Rus (Author), James Dowling (Author), Maaike van Putten (Author)
Format: Book
Published: The Company of Biologists, 2020-02-01T00:00:00Z.
Subjects:
Online Access:Connect to this object online.
Tags: Add Tag
No Tags, Be the first to tag this record!

Internet

Connect to this object online.

3rd Floor Main Library

Holdings details from 3rd Floor Main Library
Call Number: A1234.567
Copy 1 Available