Citations for
1NAIP, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
Correlation of SMN2, NAIP, p44, H4F5 and Occludin genes copy number with spinal muscular atrophy phenotype in Tunisian patients.
Amara A, Adala L, Ben Charfeddine I, Mama´ O, Mili A, Lazreg TB, H'mida D, Amri F, Salem N, Boughammura L, Saad A, Gribaa M.
Eur J Paediatr Neurol 16(2):167-74. doi: 10.1016/j.ejpn.2011.07.007. Epub 2011 Aug 6. 2012
2ACMN, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
Spinal muscular atrophy diagnostics.
Prior TW.
J Child Neurol 22(8):952-6. Review. 2007
3ACMN, SMA, SMA2, SMA3, SMA4, SMN1, SMN2
Spinal muscular atrophy: clinical classification and disease heterogeneity.
Russman BS.
J Child Neurol 22(8):946-51. Review. 2007
4SMA3, SMA4, SMN1, SMN2
Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number.
Wirth B, Brichta L, Schrank B, Lochmčller H, Blick S, Baasner A, Heller R.
Hum Genet 119(4):422-8. Epub 2006 Mar 1. 2006
5SMN1, SMA4
Gene conversion events in adult-onset spinal muscular atrophy.
Mazzei R, Gambardella A, Conforti FL, Magariello A, Patitucci A, Gabriele AL, Sprovieri T, Labate A, Valentino P, Bono F, Bonavita S, Zappia M, Muglia M, Quattrone A.
Acta Neurol Scand 109(2):151-4. 2004
6SMA, SMA3, SMA4, SMN1, SMN2
Genetic homogeneity between childhood-onset and adult-onset autosomal recessive spinal muscular atrophy.
Brahe C, Servidei S, Zappata S, Ricci E, Tonali P, Neri G.
Lancet 346(8977):741-2. 1995