Mutations of the Cav-3 gene are associated with distinct, sometimes overlapping muscle disease phenotypes. We report a new Italian family with autosomal dominant rippling muscle disease. Immunocytochemical analysis of muscle showed a deficit of caveolin-3 protein and molecular genetic analysis showed a novel mutation of the Cav-3 gene
Inherited rippling muscle disease is an autosomal dominant disorder usually associated with caveolin...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
Mutations of the Cav-3 gene are associated with distinct, sometimes overlapping muscle disease pheno...
Rippling muscle disease (RMD) is a rare muscle disorder characterised by muscle stiffness, exercise ...
Caveolin-3 is the muscle-specific protein of the caveolin family. It is expressed both in cardiac an...
Rippling muscle disease (RMD) is a rare muscle disorder characterised by muscle stiffness, exercise ...
Caveolin-3, the myocyte-specific isoform of caveolins, is preferentially expressed in skeletal, card...
Two unrelated patients with novel homozygous missense mutations (L86P and A92T) in caveolin-3 gene (...
Hereditary rippling muscle disease (RMD) is an autosomal dominant human disorder characterized by me...
Caveolins are essential proteins in caveolae architecture, small plasma membrane invaginations that ...
Mutations in the gene encoding caveolin-3 (CAV3) can cause a broad spectrum of clinical phenotypes, ...
Background: Caveolin-3 is the muscle-specific protein product of the caveolin gene family and an int...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
AbstractWe report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) assoc...
Inherited rippling muscle disease is an autosomal dominant disorder usually associated with caveolin...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
Mutations of the Cav-3 gene are associated with distinct, sometimes overlapping muscle disease pheno...
Rippling muscle disease (RMD) is a rare muscle disorder characterised by muscle stiffness, exercise ...
Caveolin-3 is the muscle-specific protein of the caveolin family. It is expressed both in cardiac an...
Rippling muscle disease (RMD) is a rare muscle disorder characterised by muscle stiffness, exercise ...
Caveolin-3, the myocyte-specific isoform of caveolins, is preferentially expressed in skeletal, card...
Two unrelated patients with novel homozygous missense mutations (L86P and A92T) in caveolin-3 gene (...
Hereditary rippling muscle disease (RMD) is an autosomal dominant human disorder characterized by me...
Caveolins are essential proteins in caveolae architecture, small plasma membrane invaginations that ...
Mutations in the gene encoding caveolin-3 (CAV3) can cause a broad spectrum of clinical phenotypes, ...
Background: Caveolin-3 is the muscle-specific protein product of the caveolin gene family and an int...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
AbstractWe report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) assoc...
Inherited rippling muscle disease is an autosomal dominant disorder usually associated with caveolin...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...
We report the first case of a heterozygous T78M mutation in the caveolin-3 gene (CAV3) associated wi...