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Brugada Syndrome: New Implications for Heterozygous Carriers of the Pathogenic SCN5A c.689T>C(p.Ile230Thr) Variant

open access: yesAmerican Journal of Medical Genetics Part A, EarlyView.
ABSTRACT Pathogenic variants in the SCN5A gene and its subunits have been identified in individuals with Brugada Syndrome. One such SCN5A variant, c.689T>C(p.Ile230Thr), was previously reported as disease‐causing only in homozygous individuals, with heterozygous carriers being unaffected.
Shayla Shojaat   +2 more
wiley   +1 more source

The effect of thoracic lateral deviation on gait parameters in blindfolded gait. [PDF]

open access: yesJ Phys Ther Sci
Komuro N   +7 more
europepmc   +1 more source

Early Thoracotomy and Decortication in Pleural Empyema. [PDF]

open access: yesCureus
Kohli A   +5 more
europepmc   +1 more source

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