| 1 | NAIP, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
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| Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.
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| Amara A, Adala L, Ben Charfeddine I, Mamaï O, Mili A, Lazreg TB, H'mida D, Amri F, Salem N, Boughammura L, Saad A, Gribaa M.
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| Eur J Paediatr Neurol 16(2):167-74. doi: 10.1016/j.ejpn.2011.07.007. Epub 2011 Aug 6.
2012
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| 2 | ACMN, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
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| Spinal muscular atrophy diagnostics.
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| Prior TW.
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| J Child Neurol 22(8):952-6. Review. 2007
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| 3 | ACMN, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
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| Spinal muscular atrophy: clinical classification and disease heterogeneity.
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| Russman BS.
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| J Child Neurol 22(8):946-51. Review. 2007
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| 4 | SMA3, SMA4, SMN1, SMN2
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| Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number.
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| Wirth B, Brichta L, Schrank B, LochmŸller H, Blick S, Baasner A, Heller R.
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| Hum Genet 119(4):422-8. Epub 2006 Mar 1. 2006
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| 5 | SMA, SMA3, SMA4, SMN1, SMN2
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| Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy.
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| Brahe C, Servidei S, Zappata S, Ricci E, Tonali P, Neri G.
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| Lancet 346(8977):741-2. 1995
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| 6 | SMA3, SMN1
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| Chronic spinal muscular atrophy in adults. 1. The Kugelberg-Welander syndrome.
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| Meadows JC, Marsden CD, Harriman DG.
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| J Neurol Sci 9(3):527-50. No abstract available. 1969
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