Associated Papers
Familial Hyperckemia and Calf Hypertrophy Secondary to a Caveolin-3 Mutation.
Otero-Loperena E et al.
American Journal of Physical Medicine & Rehabilitation, 2021
CAV3 gene sequence variations: National Genome Database and clinics.
Stavusis J et al.
Acta Neurologica Scandinavica, 2015
The role of CAV3 in long-QT syndrome: clinical and functional assessment of a caveolin-3/Kv11.1 double heterozygote versus caveolin-3 single heterozygote.
Hedley PL et al.
Circulation. Cardiovascular Genetics, 2013
Caveolinopathies: from the biology of caveolin-3 to human diseases.
Gazzerro E et al.
European Journal of Human Genetics : Ejhg, 2010
Molecular and muscle pathology in a series of caveolinopathy patients.
Fulizio L et al.
Human Mutation, 2005
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