A novel gain‐of‐function mutation in ORAI1 causes late‐onset tubular aggregate myopathy and congenital miosis
M. Garibaldi; F. Fattori; B. Riva; C. Labasse; G. Brochier; P. Ottaviani; S. Sacconi; E. Vizzaccaro; F. Laschena; N.B. Romero; A. Genazzani; E. Bertini; G. Antonini
Author Information: Unit of Neuromuscular Diseases, Department of Neurology Mental Health and Sensory Organs (NESMOS), Faculty of Medicine and Psychology
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