Homozygous Deletion in <i>KVLQT1</i> Associated With Jervell and Lange-Nielsen Syndrome - Concepedia

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Homozygous Deletion in <i>KVLQT1</i> Associated With Jervell and Lange-Nielsen Syndrome

81

Citations

24

References

1999

Year

Qiuyun Chen, Danmei Zhang, Robert L. Gingell, Arthur J. Moss, Carlo Napolitano, Silvia G. Priori, Peter J. Schwartz, Eileen Kehoe, Jennifer L. Robinson, Eric Schulze‐Bahr,

Abstract

A novel homozygous KVLQT1 mutation causes JLNS in an Amish family with deafness that is inherited as an autosomal recessive trait.

References

	Year	Citations

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