G Cordone

Mutations in the caveolin-3 gene cause autosomal dominant limb-girdle muscular dystrophy

Carlo Minetti, Federica Sotgia, Claudio Bruno et al. · Nature Genetics · 1998 · 586 citations

Life Sciences, Genetics, Molecular Genetics +7

Dystrophinopathy in isolated cases of myopathy in females

Eric P. Hoffman, Kiichi Arahata, Carlo Minetti et al. · Neurology · 1992 · 161 citations

Medicine, Neurology, Pathology +11

Mutation in the <i>CAV3</i> gene causes partial caveolin-3 deficiency and persistent elevated levels of serum creatine kinase

Ilma Floriana Carbone, Claudio Bruno, Federica Sotgia et al. · Neurology · 2000 · 157 citations

Medicine, Genetics, Molecular Genetics +17

Xeroderma pigmentosum (complementation group D) mutation is present in patients affected by trichothiodystrophy with photosensitivity

Miria Stefanini, P. Lagomarsini, C.F. Arlett et al. · Human Genetics · 1986 · 137 citations

Medicine, Dermatology, Genetics +13

Impairment of Caveolae Formation and T-System Disorganization in Human Muscular Dystrophy with Caveolin-3 Deficiency

Carlo Minetti, M. Bado, Paolo Broda et al. · American Journal Of Pathology · 2002 · 128 citations · Full text

Medicine, Molecular Medicine, Physiology +13