Mutations in the skeletal muscle α-actin gene in patients with actin myopathy and nemaline myopathy
Nigel G. Laing(Harry Perkins Institute of Medical Research), Carina Wallgren‐Pettersson(University of Helsinki), Kathryn N. North(Children's Hospital at Westmead), Imelda Hughes(Manchester University NHS Foundation Trust), Kati Donner(University of Helsinki), Atilano Lacson(University of South Florida), Duangrurdee Wattanasirichaigoon(Mahidol University), Matthew C. J. Wilce(Discovery Institute), Susan T. Iannaccone(Scottish Rite Hospital), Caroline A. Sewry(Great Ormond Street Hospital), Alan H. Beggs(Broad Institute), Christopher Verity(Addenbrooke's Hospital), Kathryn J. Swoboda(Massachusetts General Hospital), Peter Nürnberg(Cologne Excellence Cluster on Cellular Stress Responses in Aging Associated Diseases), Jaqueline Vigneron(Centre Hospitalier Régional et Universitaire de Nancy), Hans H. Goebel(University Medical Center of the Johannes Gutenberg University Mainz), Katarina Pelin(University of Helsinki), Konrad Oexle, Francesco Muntoni(Great Ormond Street Hospital), Clemens R. Müller(University of Würzburg), Rebecca Sutphen(University of South Florida), Janice R. Anderson(Addenbrooke's Hospital), Christoph Hübner(Humboldt-Universität zu Berlin), Rebecca L. Jacob(Royal Perth Hospital)
Cited by 401
Related Papers
Genotype-Phenotype Correlation in the Long-QT Syndrome
|Circulation|2001|1.8k
Missense Mutations in the Rod Domain of the Lamin A/C Gene as Causes of Dilated Cardiomyopathy and Conduction-System Disease
|New England Journal of Medicine|1999|1.4k
Mutations in ACTN4, encoding α-actinin-4, cause familial focal segmental glomerulosclerosis
|Nature Genetics|2000|1.3k