載入...
Merosin-negative congenital muscular dystrophy: Report of five cases
CONTEXT: Congenital muscular dystrophy type 1A (MDC1A) is caused by mutations in the laminin α-2 gene encoding laminin-a2. AIMS: The purpose of this study is to determine clinical and genetic results in five Turkish patients with MDC1A. SETTING AND DESIGNS: Five children with MDC1A were retrospectiv...
Na minha lista:
| 發表在: | J Pediatr Neurosci |
|---|---|
| Main Authors: | , , , |
| 格式: | Artigo |
| 語言: | Inglês |
| 出版: |
Medknow Publications & Media Pvt Ltd
2015
|
| 主題: | |
| 在線閱讀: | https://ncbi.nlm.nih.gov/pmc/articles/PMC4770646/ https://ncbi.nlm.nih.gov/pubmed/26962340 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/1817-1745.174432 |
| 標簽: |
添加標簽
沒有標簽, 成為第一個標記此記錄!
|