论文信息 - KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1 - 字舞流文

KCNQ1 mutations associated with Jervell and Lange–Nielsen syndrome and autosomal recessive Romano–Ward syndrome in India—expanding the spectrum of long QT syndrome type 1

R. Saxena | S. Bohora | T. Singh | Deepak Sharma | I. Verma | N. Namboodiri | M. Nair | R. Puri | S. Movva | Bijal Vyas | Neeraj Aggarwal | Amit Vora | Jatinder Kumar