Clinical phenotype and loss of the slow skeletal muscle troponin T in three new patients with recessive TNNT1 nemaline myopathy
Géraud, Justine, Dieterich, Klaus, Rendu, John, Uro Coste, Emmanuelle, Dobrzynski, Murielle, Marcorelle, Pascale, Ioos, Christine, Romero, Norma Beatriz, Baudou, Eloise, Brocard, Julie, Coville, AnneJournal:
Journal of Medical Genetics
DOI:
10.1136/jmedgenet-2019-106714
Date:
September, 2020
Fichier:
PDF, 997 KB
2020
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