Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients.
Pegoraro, E
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. [electronic resource] - Neurology Jul 1998 - 101-10 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0028-3878
10.1212/wnl.51.1.101 doi
Base Sequence
Biopsy
Child
Child, Preschool
DNA Mutational Analysis
Female
Fluorescent Antibody Technique
Gene Deletion
Genotype
Humans
Infant
Laminin--analysis
Male
Molecular Sequence Data
Muscle, Skeletal--chemistry
Muscular Dystrophies--congenital
Mutation
Phenotype
Polymorphism, Genetic
Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients. [electronic resource] - Neurology Jul 1998 - 101-10 p. digital
Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S.
0028-3878
10.1212/wnl.51.1.101 doi
Base Sequence
Biopsy
Child
Child, Preschool
DNA Mutational Analysis
Female
Fluorescent Antibody Technique
Gene Deletion
Genotype
Humans
Infant
Laminin--analysis
Male
Molecular Sequence Data
Muscle, Skeletal--chemistry
Muscular Dystrophies--congenital
Mutation
Phenotype
Polymorphism, Genetic