Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy
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M. Koenig | N. Romero | M. Cossée | J. Rendu | J. Fauré | J. Brocard | I. Marty | E. Lacène | K. Dieterich | A. Siegfried | C. Thèze | C. Ioos | É. Baudou | H. Pégeot | R. Juntas Morales | A. Madelaine | J. Fauré | E. Uro Coste | C. Cances | J. Geraud | M. Dobrzynski | P. Marcorelle | A. Coville
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