| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6042417 | Pediatric Neurology | 2014 | 7 Pages |
Abstract
Although lamin A/C-related congenital muscular dystrophy is a clinically distinct and recognizable phenotype, genotype/phenotype correlation, ability to anticipate onset of respiratory and cardiac involvement, and need for nutritional support remain difficult.
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Authors
LÃvia M.A. MD, PhD, Umbertina C. MD, PhD, Thais V.M.M. MS, Elisângela MS, Marco A.V. MD, PhD, Maria B.D. MD, PhD, Anne MD, Gerson MD, PhD, Edmar MD, PhD,