An autosomal dominant inherited form of HYPERTROPHIC CARDIOMYOPATHY. It results from any of more than 50 mutations involving genes encoding contractile proteins such as VENTRICULAR MYOSINS; cardiac TROPONIN T; ALPHA-TROPOMYOSIN.
See also reference (FX) in Slovak
tropomyozín troponín T myozíny komorové
See also reference (FX) in English
Tropomyosin Troponin T Ventricular Myosins
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