TY  - GEN
AU  - Weiler,T
AU  - Bashir,R
AU  - Anderson,L V
AU  - Davison,K
AU  - Moss,J A
AU  - Britton,S
AU  - Nylen,E
AU  - Keers,S
AU  - Vafiadaki,E
AU  - Greenberg,C R
AU  - Bushby,C R
AU  - Wrogemann,K
TI  - Identical mutation in patients with limb girdle muscular dystrophy type 2B or Miyoshi myopathy suggests a role for modifier gene(s)
SN  - 0964-6906
PY  - 1999///0623
KW  - Base Sequence
KW  - Biopsy
KW  - Canada
KW  - Dysferlin
KW  - Female
KW  - Haplotypes
KW  - Homozygote
KW  - Humans
KW  - Indians, North American
KW  - genetics
KW  - Male
KW  - Membrane Proteins
KW  - Molecular Sequence Data
KW  - Muscle Proteins
KW  - Muscle, Skeletal
KW  - metabolism
KW  - Muscular Dystrophies
KW  - Mutation
KW  - Mutation, Missense
KW  - Pedigree
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1093/hmg/8.5.871
ER  -