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References in periodicals archive ?
Categorization of the congenital mutations in Romano-Ward Syndrome is based on a numbering scheme with several mutations identified with types 1-3 being the most common forms seen.
Romano-Ward syndrome is the most common inherited form of LQTS and is transmitted as an autosomal-dominant trait[1,2.5,6]; gene carriers are expected to be clinically affected (ie, they have evidence of LQTS) and have a 50% likelihood of transmitting the disease-causing gene to their offspring.