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...

Täydet tiedot

Bibliografiset tiedot

Päätekijät:	Imen Rekik, Amir Boukhris, Sourour Ketata, Mohamed Amri, Nourhene Essid, Imed Feki, Chokri Mhiri
Aineistotyyppi:	Artigo
Kieli:	Inglês
Julkaistu:	Wolters Kluwer Medknow Publications 2013-01-01
Sarja:	Annals of Indian Academy of Neurology
Aiheet:	Neuronal apoptosis inhibitory protein (NAIP) gene spinal muscular atrophy survival motor neuron (SMN) gene
Linkit:	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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