Author:
Theodorou L.,Nicolaou P.,Koutsou P.,Georghiou A.,Anastasiadou V.,Tanteles G.,Kyriakides T.,Zamba-Papanicolaou E.,Christodoulou K.
Publisher
Springer Science and Business Media LLC
Subject
Psychiatry and Mental health,Clinical Neurology,Dermatology,General Medicine
Reference31 articles.
1. Ogino S, Wilson RB, Gold B (2004) New insights on the evolution of the SMN1 and SMN2 region: simulation and meta-analysis for allele and haplotype frequency calculations. Eur J Hum Genet 12(12):1015–1023. doi: 10.1038/sj.ejhg.5201288
2. Markowitz JA, Singh P, Darras BT (2012) Spinal muscular atrophy: a clinical and research update. Pediatr Neurol 46(1):1–12. doi: 10.1016/j.pediatrneurol.2011.09.001
3. D’Amico A, Mercuri E, Tiziano FD, Bertini E (2011) Spinal muscular atrophy. Orphanet J Rare Dis 6:71. doi: 10.1186/1750-1172-6-71
4. Prior TW, Krainer AR, Hua Y, Swoboda KJ, Snyder PC, Bridgeman SJ, Burghes AH, Kissel JT (2009) A positive modifier of spinal muscular atrophy in the SMN2 gene. Am J Hum Genet 85(3):408–413. doi: 10.1016/j.ajhg.2009.08.002
5. Clermont O, Burlet P, Burglen L, Lefebvre S, Pascal F, McPherson J, Wasmuth JJ, Cohen D, Le Paslier D, Weissenbach J et al (1994) Use of genetic and physical mapping to locate the spinal muscular atrophy locus between two new highly polymorphic DNA markers. Am J Hum Genet 54(4):687–694
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