Genetic and expression studies of <it>SMN2 </it>gene in Russian patients with spinal muscular atrophy type II and III
<p>Abstract</p> <p>Background</p> <p>Spinal muscular atrophy (SMA type I, II and III) is an autosomal recessive neuromuscular disorder caused by mutations in the survival motor neuron gene (<it>SMN1</it>). <it>SMN2 </it>is a centromeric copy gene...
Main Authors: | , , , , , , , |
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Format: | Article |
Language: | English |
Published: |
BMC
2011-07-01
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Series: | BMC Medical Genetics |
Online Access: | http://www.biomedcentral.com/1471-2350/12/96 |