Author:
Tawil Rabi,Mah Jean K.,Baker Scott,Wagner Kathryn R.,Ryan Monique M.,Baker Scott,Corbett Alistair,van Engelen Baziel,McNamara Stephen,Mah Jean K.,Ryan Monique M.,Rasko John,Raykar Veena,Sacconi Sabrina,Tapscott Stephen J.,Tawil Rabi,Wagner Kathryn R.,Watts Alan
Funder
FSHD Global Research Foundation
Subject
Genetics(clinical),Clinical Neurology,Neurology,Pediatrics, Perinatology, and Child Health
Reference36 articles.
1. Evidence-based guideline summary: evaluation, diagnosis, and management of facioscapulohumeral muscular dystrophy;Tawil;Neurology,2015
2. Genetic and epigenetic contributors to FSHD;Daxinger;Curr Opin Genet Dev,2015
3. Facioscapulohumeral dystrophy: the path to consensus on pathophysiology;Tawil;Skelet Muscle,2014
4. 171st ENMC international workshop: standards of care and management of facioscapulohumeral muscular dystrophy;Tawil;Neuromuscul Disord,2010
5. Best practice guidelines on genetic diagnostics of facioscapulohumeral muscular dystrophy: workshop. 9th June 2010, LUMC, Leiden, The Netherlands;Lemmers;Neuromuscul Disord,2012
Cited by
7 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