Molecular analysis of the SMN and NAIP genes in Iranian spinal muscular atrophy patients

Background: Spinal muscular atrophy (SMA) is an autosomal recessive neuromuscular disorder characterized by degeneration of spinal cord anterior horn cells, leading to muscular atrophy. SMA is clinically classified into three subgroups based on the age of onset and severity. The majority of patient...

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Veröffentlicht in:	Pediatrics international 2009-04, Vol.51 (2), p.193-196
Hauptverfasser:	Omrani, Omid, Bonyadi, Morteza, Barzgar, Mohammad
Format:	Artikel
Sprache:	eng
Schlagworte:	Child Gene Deletion Genes Humans Iran Iranian population NAIP gene Neuromuscular diseases Neuronal Apoptosis-Inhibitory Protein - genetics Pediatrics Prenatal Diagnosis SMN Complex Proteins - genetics SMN Complex Proteins - metabolism SMN gene Spinal Muscular Atrophies of Childhood - genetics spinal muscular atrophy
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