TY  - GEN
AU  - Pegoraro,E
AU  - Marks,H
AU  - Garcia,C A
AU  - Crawford,T
AU  - Mancias,P
AU  - Connolly,A M
AU  - Fanin,M
AU  - Martinello,F
AU  - Trevisan,C P
AU  - Angelini,C
AU  - Stella,A
AU  - Scavina,M
AU  - Munk,R L
AU  - Servidei,S
AU  - Bönnemann,C C
AU  - Bertorini,T
AU  - Acsadi,G
AU  - Thompson,C E
AU  - Gagnon,D
AU  - Hoganson,G
AU  - Carver,V
AU  - Zimmerman,R A
AU  - Hoffman,E P
TI  - Laminin alpha2 muscular dystrophy: genotype/phenotype studies of 22 patients
SN  - 0028-3878
PY  - 1998///0730
KW  - Base Sequence
KW  - Biopsy
KW  - Child
KW  - Child, Preschool
KW  - DNA Mutational Analysis
KW  - Female
KW  - Fluorescent Antibody Technique
KW  - Gene Deletion
KW  - Genotype
KW  - Humans
KW  - Infant
KW  - Laminin
KW  - analysis
KW  - Male
KW  - Molecular Sequence Data
KW  - Muscle, Skeletal
KW  - chemistry
KW  - Muscular Dystrophies
KW  - congenital
KW  - Mutation
KW  - Phenotype
KW  - Polymorphism, Genetic
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1212/wnl.51.1.101
ER  -