Author:
Pagliarini Vittoria,La Rosa Piergiorgio,Sette Claudio
Funder
Association for International Cancer Research (AICR)
Associazione Italiana Ricerca sul Cancro (AIRC)
Fondazione Telethon (IT)
Fondazione Umberto Veronesi
Publisher
Springer Science and Business Media LLC
Subject
Genetics(clinical),Genetics
Reference220 articles.
1. Aartsma-Rus A, Ginjaar IB, Bushby K (2016) The importance of genetic diagnosis for Duchenne muscular dystrophy. J Med Genet 53:145–151
2. Abu-Baker A, Rouleau GA (2007) Oculopharyngeal muscular dystrophy: recent advances in the understanding of the molecular pathogenic mechanisms and treatment strategies. Biochem Biophys Acta 1772:173–185
3. Adachi K, Takeshima Y, Wada H, Yagi M, Nakamura H, Matsuo M (2003) Heterogous dystrophin mRNA produced by a novel splice acceptor site mutation in intermediate dystrophinopathy. Pediatr Res 53:125–131
4. Anderson SL, Coli R, Daly IW, Kichula EA, Rork MJ, Volpi SA, Ekstein J, Rubin BY (2001) Familial dysautonomia is caused by mutations of the IKAP gene. Am J Hum Genet 68:753–758
5. Andreadis A, Brown WM, Kosik KS (1992) Structure and novel exons of the human tau gene. Biochemistry 31:10626–10633
Cited by
14 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