TY  - GEN
AU  - Pegoraro,E
AU  - Fanin,M
AU  - Trevisan,C P
AU  - Angelini,C
AU  - Hoffman,E P
TI  - A novel laminin alpha2 isoform in severe laminin alpha2 deficient congenital muscular dystrophy
SN  - 0028-3878
PY  - 2000///1207
KW  - Adolescent
KW  - Alternative Splicing
KW  - Exons
KW  - Female
KW  - Humans
KW  - Laminin
KW  - analysis
KW  - Magnetic Resonance Imaging
KW  - Muscles
KW  - chemistry
KW  - Muscular Dystrophies
KW  - congenital
KW  - Mutation
KW  - genetics
KW  - Phenotype
KW  - Protein Isoforms
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.55.8.1128
ER  -