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S00380-013-0406-2
S00380-013-0406-2
http://dx.doi.org/10.1007/S00380-013-0406-2
Congenital long QT syndrome with compound mutations in the KCNH2 gene.
P356
Q33163304-005FAC94-B988-46A3-BB02-2522A53AB3FD
P356
S00380-013-0406-2
http://dx.doi.org/10.1007/S00380-013-0406-2