Clinical and molecular aspects of the myotonic dystrophies: a review.
Type 1 myotonic dystrophy or DM1 (Steinert's disease), which is the commonest muscular dystrophy in adults, has intrigued physicians for over a century. Unusual features, compared with other dystrophies, include myotonia, anticipation, and involvement of other organs, notably the brain, eyes, s...
Main Authors: | Machuca-Tzili, L, Brook, D, Hilton-Jones, D |
---|---|
Format: | Journal article |
Language: | English |
Published: |
2005
|
Similar Items
-
Molecular genetics of myotonic dystrophy.
by: Barnes, P, et al.
Published: (1993) -
Myotonic dystrophy--forgotten aspects of an often neglected condition.
by: Hilton-Jones, D
Published: (1997) -
The myotonic dystrophies: diagnosis and management.
by: Turner, C, et al.
Published: (2010) -
Disrupting the Molecular Pathway in Myotonic Dystrophy
by: Xiaomeng Xing, et al.
Published: (2021-12-01) -
Myotonic dystrophy: diagnosis, management and new therapies.
by: Turner, C, et al.
Published: (2014)