Troponin T1
National Institutes of Health
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Recessive null variants of the slow skeletal muscle troponin T1 (TNNT1) gene are a rare cause of nemaline myopathy that is fatal…
Sources/description: Expressed sequence tags, European Molecular Biology Laboratory (EMBL) accession numbers AJ301262, AJ301107…
The term “congenital myopathy” is applied to muscle disorders presenting in infancy with generalized muscle weakness and…