Variable clinical phenotype in merosin-deficient congenital muscular dystrophy associated with differential immunolabelling of two fragments of the laminin α2 chain
- 31 May 1997
- journal article
- Published by Elsevier in Neuromuscular Disorders
- Vol. 7 (3) , 169-175
- https://doi.org/10.1016/s0960-8966(97)00425-2
Abstract
No abstract availableKeywords
This publication has 0 references indexed in Scilit: