TY  - GEN
AU  - Sewry,C A
AU  - Naom,I
AU  - D'Alessandro,M
AU  - Sorokin,L
AU  - Bruno,S
AU  - Wilson,L A
AU  - Dubowitz,V
AU  - Muntoni,F
TI  - Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin alpha 2 chain
SN  - 0960-8966
PY  - 1997///0728
KW  - Antibody Specificity
KW  - Biopsy
KW  - Child
KW  - Child, Preschool
KW  - Female
KW  - Genetic Linkage
KW  - Humans
KW  - Immunohistochemistry
KW  - Laminin
KW  - deficiency
KW  - Male
KW  - Muscle, Skeletal
KW  - chemistry
KW  - Muscular Dystrophies
KW  - congenital
KW  - Phenotype
N1  - Publication Type: Journal Article; Research Support, Non-U.S. Gov't
UR  - https://doi.org/10.1016/s0960-8966(97)00425-2
ER  -