Clinical, histological and genetic characterization of reducing body myopathy caused by mutations in FHL1.
Joachim Schessl; Ana L. Taratuto; Caroline Sewry; Roberta Battini; Steven S. Chin; Baijayanta Maiti; Alberto L. Dubrovsky; Marcela G. Erro; Graciela Espada; Monica Robertella; Maria Saccoliti; Patricia Olmos; Leslie R. Bridges; Peter Standring; Ying Hu; Yaqun Zou; Kathryn J. Swoboda; Mena Scavina; Hans-Hilmar Goebel; Christina A. Mitchell; Brain: A Journal of Neurology, 2009, vol. 132, issue 2, p 452, ISSN 00068950. ISBN 14602156.

Full Text Resources Located for this Citation

View article on EBSCOhost(Login required)
View article via CrossRef