Clinical and molecular findings in a cohort of ANO5‐related myopathy

Clinical and molecular findings in a cohort of ANO5‐related myopathy

Abstract Objective ANO5‐related myopathy is an important cause of limb‐girdle muscular dystrophy (LGMD) and hyperCKemia. The main descriptions have emerged from European cohorts, and the burden of the disease worldwide is unclear. We provide a detailed characterization of a large Brazilian cohort of...

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Main Authors: André M. S. Silva, Antônio R. Coimbra-Neto, Paulo Victor S. Souza, Pablo B. Winckler, Marcus V. M. Gonçalves, Eduardo B. U. Cavalcanti, Alzira A. D. S. Carvalho, Cláudia F. D. R. Sobreira, Clara G. Camelo, Rodrigo D. H. Mendonça, Eduardo D. P. Estephan, Umbertina C. Reed, Marcela C. Machado-Costa, Mario E. T. Dourado-Junior, Vanessa C. Pereira, Marcelo M. Cruzeiro, Paulo V. P. Helito, Laís U. Aivazoglou, Leonardo V. D. Camargo, Hudson H. Gomes, Amaro J. S. D. Camargo, Wladimir B. V. D. R. Pinto, Bruno M. L. Badia, Luiz H. Libardi, Mario T. Yanagiura, Acary S. B. Oliveira, Anamarli Nucci, Jonas A. M. Saute, Marcondes C. França-Junior, Edmar Zanoteli
Format: Article
Language:English
Published: Wiley 2019-07-01
Series:Annals of Clinical and Translational Neurology
Online Access:https://doi.org/10.1002/acn3.50801

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