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Deletion analysis of SMN and NAIP genes in Tunisian patients with spinal muscular atrophy
BACKGROUND: Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder involving degeneration of anterior horn cells of spinal cord, resulting in progressive muscle weakness and atrophy. AIMS: The purpose of our study was to determine the frequency of SMN and NAIP deletions in Tu...
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| 主要な著者: | , , , , , , |
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| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Medknow Publications & Media Pvt Ltd
2013
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3644783/ https://ncbi.nlm.nih.gov/pubmed/23661964 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.4103/0972-2327.107704 |
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