Central core disease. A correlated genetic, histochemical, ultramicroscopic, and biochemical study.
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Central core diseaseCharacterization and temporal development of cores in a mouse model of malignant hyperthermiaThe I4895T mutation in the type 1 ryanodine receptor induces fiber-type specific alterations in skeletal muscle that mimic premature aging.Excitation--contraction uncoupling by a human central core disease mutation in the ryanodine receptor.Teaching monograph: pathology of skeletal muscle diseases.Missense mutations in the beta-myosin heavy-chain gene cause central core disease in hypertrophic cardiomyopathyFunctional effects of central core disease mutations in the cytoplasmic region of the skeletal muscle ryanodine receptorLate components of motor unit potentials in central core diseaseSingle fibre electromyography in central core disease.Mutations in the nebulin gene in a child with nemaline (rod) myopathy.
P2860
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P2860
Central core disease. A correlated genetic, histochemical, ultramicroscopic, and biochemical study.
description
article científic
@ca
article scientifique
@fr
articolo scientifico
@it
artigo científico
@pt
bilimsel makale
@tr
scientific article published on December 1975
@en
vedecký článok
@sk
vetenskaplig artikel
@sv
videnskabelig artikel
@da
vědecký článek
@cs
name
Central core disease. A correl ...... scopic, and biochemical study.
@en
Central core disease. A correl ...... scopic, and biochemical study.
@nl
type
label
Central core disease. A correl ...... scopic, and biochemical study.
@en
Central core disease. A correl ...... scopic, and biochemical study.
@nl
prefLabel
Central core disease. A correl ...... scopic, and biochemical study.
@en
Central core disease. A correl ...... scopic, and biochemical study.
@nl
P2093
P2860
P356
P1476
Central core disease. A correl ...... scopic, and biochemical study.
@en
P2093
Badenhorst M
Heffron JJ
P2860
P304
P356
10.1136/JNNP.38.12.1177
P407
P577
1975-12-01T00:00:00Z