CONGENITAL MYOPATHIES: NEMALINE AND TITINOPATHIES: P.232Core and rod myopathy due to a novel mutation in BTB domain of KBTBD13 gene presenting as LGMD. - Garibaldi, M.; Fattori, F.; Bortolotti, C.; Brochier, G.; Labasse, C.; Verardo, M.; Bertini, E.; Pennisi, E.; Paradas, C.; Romero, N.; Antonini, G. (Neuromuscular Disorders, 2018)