Molecular analysis of the SMN and NAIP genes in Saudi spinal muscular atrophy patients
Author:
Publisher
Elsevier BV
Subject
Neurology (clinical),Neurology
Reference18 articles.
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3. Large scale deletions of the 5q13 region are specific to Werdnig–Hoffmann disease;Burlet;J Med Genet,1996
4. Deletion analysis of SMN and NAIP gene in spinal muscular atrophy Italian families;Capon;Muscle Nerve,1996
5. Molecular basis of spinal muscular atrophy in Chinese;Chang;Am J Hum Genet,1995
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