Author:
Toscano A.,Vitiello L.,Comi G.P.,Galvagni F.,Miorin M.,Prelle A.,Fortunato F.,Bardoni A.,Mora M.,Fiumara A.,Falsaperla R.,Tomelleri G.,Tonin P.,Danieli G.A.,Vita G.
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference32 articles.
1. The molecular basis for Duchenne versus Becker muscular dystrophy: correlation of severity with type of deletion;Koenig;Am J Hum Genet,1989
2. A novel nonsense mutation in the human dystrophin gene;Saad;Hum Mutation,1993
3. A possible missense mutation detected in the dystrophin gene by double strand conformation analysis (DSCA);Saad;Neuromusc Disord,1994
4. Topography of the Duchenne muscular dystrophy (DMD) gene: FIGE and cDNA analysis of 194 cases reveals 115 deletions and 13 duplications;Den Dunnen;Am J Hum Genet,1989
5. Duplication mutation at the Duchenne muscular dystrophy locus: its frequency, distribution, origin, and phenotype-genotype correlation;Hu;Am J Hum Genet,1990
Cited by
8 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