Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy.
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Hypertrophic Cardiomyopathy Cardiac Troponin C Mutations Differentially Affect Slow Skeletal and Cardiac Muscle Regulation.The novel αB-crystallin (CRYAB) mutation p.D109G causes restrictive cardiomyopathy.Myofilament Calcium Sensitivity: Consequences of the Effective Concentration of Troponin I.Pathogenesis of depression- and anxiety-like behavior in an animal model of hypertrophic cardiomyopathy.Structural consequences of mutations associated with idiopathic restrictive cardiomyopathy.Myosin Rod Hypophosphorylation and CB Kinetics in Papillary Muscles from a TnC-A8V KI Mouse Model.
P2860
Evidence for troponin C (TNNC1) as a gene for autosomal recessive restrictive cardiomyopathy with fatal outcome in infancy.
description
2016 nî lūn-bûn
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2016年の論文
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年学术文章
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2016年學術文章
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2016年學術文章
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2016年學術文章
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name
Evidence for troponin C (TNNC1 ...... with fatal outcome in infancy.
@en
Evidence for troponin C
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type
label
Evidence for troponin C (TNNC1 ...... with fatal outcome in infancy.
@en
Evidence for troponin C
@nl
prefLabel
Evidence for troponin C (TNNC1 ...... with fatal outcome in infancy.
@en
Evidence for troponin C
@nl
P2093
P2860
P50
P356
P1476
Evidence for troponin C (TNNC1 ...... with fatal outcome in infancy
@en
P2093
Ewa Michalak
Maria Franaszczyk
Piotr Stawinski
Tomasz M Ksiazczyk
P2860
P304
P356
10.1002/AJMG.A.37860
P407
P50
P577
2016-09-08T00:00:00Z