Cardiology MCQ 002

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Familial hypertrophic cardiomyopathy is most likely to be secondary to a mutation in:

a) myosin regulatory proteins
b) myosin binding protein-C
c) Myosin light chains
Hypertrophic Cardiomyopathy: For Patients, Their Families and Interested Physiciansd) Troponin I
e) Troponin T

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Category: Cardiology MCQs

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