| 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, Mamaļ 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 | SMN1, SMA2
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| Preservation of central motor conduction in patients with spinal muscular atrophy type II.
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| Imai T, Matsuya M, Matsumoto H, Ishikawa Y, Minami R.
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| Brain Dev 17(6):432-5. 1995
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| 5 | SMN1, SMA2
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| Spinal muscular atrophy type II. A separate genetic and clinical entity from type I (Werdnig-Hoffmann disease) and type 3 (Kugelberg-Welander disease).
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| Fried K, Emery AE.
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| Clin Genet 2(4):203-9. No abstract available. 1971
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