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

Nature Genetics

Volumn 18, Issue 4, 1998, Pages 365-368

  Minetti, C ^a   Sotgia, F ^a   Bruno, C ^a   Scartezzini, P ^a   Broda, P ^a   Bado, M ^a   Masetti, E ^a   Mazzocco, M ^a   Egeo, A ^a   Donati, M A ^a   Volonte, D ^a   Galbiati, F ^a   Cordone, G ^a   Bricarelli, F D ^a   Lisanti, M P ^a   Zara, F ^a  

^a UNIVERSITY OF GENOA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

CAVEOLIN;

AMINO ACID SEQUENCE; ARTICLE; CHROMOSOME 1Q; CHROMOSOME 5Q; CLINICAL ARTICLE; CLINICAL TRIAL; CONTROLLED STUDY; GENE ISOLATION; GENE LOCATION; GENETIC SCREENING; HUMAN; HUMAN CELL; LIMB GIRDLE MUSCULAR DYSTROPHY; MISSENSE MUTATION; MUSCLE BIOPSY; MUSCLE HYPERTROPHY; MUSCLE WEAKNESS; NUCLEOTIDE SEQUENCE; PRIORITY JOURNAL; PROTEIN ANALYSIS; PROTEIN EXPRESSION; STRUCTURE ACTIVITY RELATION;

ADOLESCENT; ADULT; AGED; AMINO ACID SEQUENCE; AMINO ACID SUBSTITUTION; BLOTTING, WESTERN; CAVEOLIN 3; CAVEOLINS; CHILD; CHROMOSOMES, HUMAN, PAIR 3; DNA, COMPLEMENTARY; FAMILY HEALTH; FEMALE; GENES, DOMINANT; HETEROZYGOTE; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MEMBRANE PROTEINS; MIDDLE AGED; MOLECULAR SEQUENCE DATA; MUSCLE, SKELETAL; MUSCULAR DYSTROPHIES; MUTATION; PEDIGREE; SEQUENCE HOMOLOGY, AMINO ACID;

EID: 0031920515     PISSN: 10614036     EISSN: None     Source Type: Journal    
DOI: 10.1038/ng0498-365     Document Type: Article

References (30)