Author:
Willis Tracey A.,Hollingsworth Kieren G.,Coombs Anna,Sveen Marie-Louise,Andersen Søren,Stojkovic Tanya,Eagle Michelle,Mayhew Anna,de Sousa Paulo L.,Dewar Liz,Morrow Jasper M.,Sinclair Christopher D. J.,Thornton John S.,Bushby Kate,Lochmüller Hanns,Hanna Michael G.,Hogrel Jean-Yves,Carlier Pierre G.,Vissing John,Straub Volker
Publisher
Public Library of Science (PLoS)
Reference23 articles.
1. FKRP (826C>A) frequently causes limb-girdle muscular dystrophy in German patients. J Med Genet;MC Walter,2004
2. Mutations in the fukutin related protein gene (FKRP) identify limb girdle muscular dystrophy 2I as a milder allelic variant of congenital muscular dystrophy MDC1C. Hum Mol Genet;M Brockington,2001
3. Prevalence of genetic muscle disease in Northern England: in-depth analysis of a muscle clinic population;FL Norwood;Brain,2009
4. The phenotype of limb girdle muscular dystrophy 2I;M Poppe;Neurology,2003
5. The 105th ENMC sponsored workshop: pathogenesis in the non-sarcoglycan limb-girdle muscular dystrophies, Naarden, April 12–14, 2002;K Bushby;Neuromuscul Disord,2003
Cited by
151 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