Open AccessThe expanding clinical and genetic spectrum of the myotonic dystrophies
Author(s) -
K. Ricker
Publication year - 2001
Publication title -
neurology bulletin
Language(s) - English
Resource type - Journals
eISSN - 2304-3067
pISSN - 1027-4898
DOI - 10.17816/nb79796
Subject(s) - myotonic dystrophy , spectrum (functional analysis) , medicine , genetics , biology , physics , quantum mechanics
The main clinical features of dominantly inherited myotonic dystrophies are myotonia, muscle weakness, and cataracts.
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