Concepedia

Long QT syndrome with compound mutations is associated with a more severe phenotype: A Japanese multicenter study

Hideki Itoh, Wataru Shimizu, Kenshi Hayashi, Kenichiro Yamagata, Tomoko Sakaguchi, Seiko Ohno, Takeru Makiyama, Masaharu Akao, Tomohiko Ai, Takashi Noda,

Heart Rhythm · 2010 · 110 citations · 28 references

DOI

Concepts

References

28

An analysis of the time-relations of electrocardiograms

H. C. Bazett · 1920 · 3.8K citations

, , +10

Cardiac Electrophysiology: From Cell to Bedside

Annals of Internal Medicine · 1991 · 2.4K citations

, , +14

Congenital deaf-mutism, functional heart disease with prolongation of the Q-T interval, and sudden death

A Jervell, F Lange-Nielsen · American Heart Journal · 1957 · 1.6K citations

, , +15

A novel mutation in the potassium channel gene KVLQT1 causes the Jervell and Lange-Nielsen cardioauditory syndrome

Nathalie Neyroud, Frédérique Tesson, Isabelle Denjoy et al. · Nature Genetics · 1997 · 883 citations

, , +16

A NEW FAMILIAL CARDIAC SYNDROME IN CHILDREN.

Ward Oc · PubMed · 1964 · 832 citations

, , +10