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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...
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| Pubblicato in: | J Pediatr Neurosci |
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| Autori principali: | , , , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
Medknow Publications & Media Pvt Ltd
2015
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| Soggetti: | |
| Accesso online: | 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 |
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