Mutational analysis of SMN gene in patients with spinal muscular atrophy and the correlation between mutation and the severity of clinical manifestations
<b>Objective:</b> studying of mutations in the SMN1, SMN2 and NAIP genes in the diagnosis of spinal muscular atrophy and determining the correlation between the mutation and the severity of clinical manifestations.<br> <b>Methods:</b> 82 children with suspicion of spina...
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National Scientific Medical Center,
2017-09-01T00:00:00Z.
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A1234.567 |
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