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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Detalles Bibliográficos
Autores principales: Rekik, Imen, Boukhris, Amir, Ketata, Sourour, Amri, Mohamed, Essid, Nourhene, Feki, Imed, Mhiri, Chokri
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2013
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644783/
https://www.ncbi.nlm.nih.gov/pubmed/23661964
http://dx.doi.org/10.4103/0972-2327.107704

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3644783/
https://www.ncbi.nlm.nih.gov/pubmed/23661964
http://dx.doi.org/10.4103/0972-2327.107704

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