Author:
Vignoli Aglaia,Borgatti Renato,Peron Angela,Zucca Claudio,Ballarati Lucia,Bonaglia Clara,Bellini Melissa,Giordano Lucio,Romaniello Romina,Bedeschi Maria Francesca,Epifanio Roberta,Russo Silvia,Caselli Rossella,Giardino Daniela,Darra Francesca,La Briola Francesca,Banderali Giuseppe,Canevini Maria Paola
Subject
Clinical Neurology,Neurology
Reference30 articles.
1. Methylation of HpaII and HhaI sites near the polymorphic CAG repeat in the human androgen-receptor gene correlates with X chromosome inactivation;Allen;Am J Hum Genet,1992
2. Rett syndrome is caused by mutations in X-linked MECP2, encoding methyl-CpG-binding protein 2;Amir;Nat Genet,1999
3. X-linked mental retardation syndrome with short stature, small hands and feet, seizures, cleft palate, and glaucoma is linked to Xq28;Armfield;Am J Hum Genet,1999
4. Four unrelated patients with Lubs X-linked mental retardation syndrome and different Xq28 duplications;Bartsch;Am J Med Genet A,2010
5. Revised terminology and concepts for organization of seizures and epilepsies: report of the ILAE Commission on Classification and Terminology, 2005-2009;Berg;Epilepsia,2010
Cited by
34 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