TY  - GEN
AU  - Richard,I
AU  - Brenguier,L
AU  - Dinçer,P
AU  - Roudaut,C
AU  - Bady,B
AU  - Burgunder,J M
AU  - Chemaly,R
AU  - Garcia,C A
AU  - Halaby,G
AU  - Jackson,C E
AU  - Kurnit,D M
AU  - Lefranc,G
AU  - Legum,C
AU  - Loiselet,J
AU  - Merlini,L
AU  - Nivelon-Chevallier,A
AU  - Ollagnon-Roman,E
AU  - Restagno,G
AU  - Topaloglu,H
AU  - Beckmann,J S
TI  - Multiple independent molecular etiology for limb-girdle muscular dystrophy type 2A patients from various geographical origins
SN  - 0002-9297
PY  - 1997///0603
KW  - Adolescent
KW  - Adult
KW  - Age of Onset
KW  - Calpain
KW  - genetics
KW  - Child
KW  - Child, Preschool
KW  - Chromosomes, Human, Pair 15
KW  - Europe
KW  - Female
KW  - Genetic Heterogeneity
KW  - Genetic Markers
KW  - Haplotypes
KW  - Humans
KW  - Isoenzymes
KW  - Lod Score
KW  - Male
KW  - Middle East
KW  - Muscle Proteins
KW  - Muscular Dystrophies
KW  - classification
KW  - Mutation
KW  - Pedigree
KW  - United States
N1  - Publication Type: Comparative Study; Journal Article; Research Support, Non-U.S. Gov't
ER  -