Author:
Zernov N. V.,Marakhonov A. V.,Vyakhireva J. V.,Guskova A. A.,Dadali E. L.,Skoblov M. Yu.
Reference71 articles.
1. Padberg, G.W., Frants, R.R., Brouwer, O.F., et al., Facioscapulohumeral muscular dystrophy in the Dutch population, Muscle Nerve Suppl., 1995, vol. 2, pp. S81–S84.
2. Flanigan, K.M., Coffeen, C.M., Sexton, L., et al., Genetic characterization of a large, historically significant Utah kindred with facioscapulohumeral dystrophy, Neuromuscular Disord., 2001, vol. 11, nos. 6–7, pp. 525–529.
3. Mostacciuolo, M.L., Pastorello, E., Vazza, G., et al., Facioscapulohumeral muscular dystrophy: epidemiological and molecular study in a north-east Italian population sample, Clin. Genet., 2009, vol. 75, no. 6, pp. 550–555. doi 10.1111/j.1399-0004.2009.01158.x
4. Norwood, F.L., Harling, C., Chinnery, P.F., et al., Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population, Brain, 2009, vol. 132, no. 11, pp. 3175–3186. doi 10.1093/brain/awp236
5. Zatz, M., Marie, S.K., Passos-Bueno, M.R., et al., High proportion of new mutations and possible anticipation in Brazilian facioscapulohumeral muscular dystrophy families, Am. J. Hum. Genet., 1995, vol. 56, no. 1, pp. 99–105.
Cited by
2 articles.
订阅此论文施引文献
订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献