TY  - GEN
AU  - Pegoraro,E
AU  - Mancias,P
AU  - Swerdlow,S H
AU  - Raikow,R B
AU  - Garcia,C
AU  - Marks,H
AU  - Crawford,T
AU  - Carver,V
AU  - Di Cianno,B
AU  - Hoffman,E P
TI  - Congenital muscular dystrophy with primary laminin alpha2 (merosin) deficiency presenting as inflammatory myopathy
SN  - 0364-5134
PY  - 1997///0123
KW  - Base Sequence
KW  - Biopsy
KW  - Child
KW  - Child, Preschool
KW  - Deoxyribonucleases, Type II Site-Specific
KW  - Electromyography
KW  - Female
KW  - Humans
KW  - Infant
KW  - Infant, Newborn
KW  - Inflammation
KW  - Laminin
KW  - deficiency
KW  - Middle Aged
KW  - Motor Activity
KW  - Muscle, Skeletal
KW  - pathology
KW  - Muscular Dystrophies
KW  - congenital
KW  - Nuclear Family
KW  - Pedigree
KW  - Point Mutation
KW  - Polymerase Chain Reaction
KW  - Polymorphism, Restriction Fragment Length
KW  - Polymorphism, Single-Stranded Conformational
KW  - Polymyositis
KW  - physiopathology
KW  - Sequence Deletion
N1  - Publication Type: Case Reports; Journal Article; Research Support, U.S. Gov't, P.H.S
UR  - https://doi.org/10.1002/ana.410400515
ER  -