Protein Structure-Function Relationship at Work: Learning from Myopathy Mutations of the Slow Skeletal Muscle Isoform of Troponin T
Author:
Funder
National Institutes of Health
Publisher
Frontiers Media SA
Subject
Physiology (medical),Physiology
Reference100 articles.
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3. Functional basis of three new recessive mutations of slow skeletal muscle troponin T found in non-amish TNNT1 nemaline myopathies;Amarasinghe;Biochemistry,2016
4. N-Terminal hypervariable region of muscle type isoforms of troponin T differentially modulates the affinity of tropomyosin-binding site 1;Amarasinghe;Biochemistry,2015
5. Molecular basis of human cardiac troponin T isoforms expressed in the developing, adult, and failing heart;Anderson;Circ. Res.,1995
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