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...
Furkejuvvon:
| Váldodahkkit: | , , , , , , |
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| Materiálatiipa: | Artigo |
| Giella: | Inglês |
| Almmustuhtton: |
Wolters Kluwer Medknow Publications
2013-01-01
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| Ráidu: | Annals of Indian Academy of Neurology |
| Fáttát: | |
| Liŋkkat: | http://www.annalsofian.org/article.asp?issn=0972-2327;year=2013;volume=16;issue=1;spage=57;epage=61;aulast=Rekik |
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