IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome-Reference-Cited by-同舟云学术

IsK and KvLQT1: Mutation in Either of the Two Subunits of the Slow Component of the Delayed Rectifier Potassium Channel Can Cause Jervell and Lange-Nielsen Syndrome

Published:1997-11-01 Issue:12 Volume:6 Page:2179-2185
ISSN:0964-6906
Container-title:Human Molecular Genetics
language:en
Short-container-title:Human Molecular Genetics

Author:

Tyson J.,Tranebjaerg L.,Bellman S.,Wren C.,Taylor J. F. N.,Bathen J.,Aslaksen B.,Sorland S. J.,Lund O.,Malcolm S.,Pembrey M.,Bhattacharya S.,Bitner-Glindzicz M.

Publisher

Oxford University Press (OUP)

Subject

Genetics (clinical),Genetics,Molecular Biology,General Medicine

Link

http://academic.oup.com/hmg/article-pdf/6/12/2179/6956214/6-12-2179.pdf

Reference33 articles.

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

2. Genes and deafness

3. Hereditary Inner-Ear Abnormalities in Animals: Relationships With Human Abnormalities

4. Pathology of the Ear in the Cardio-Auditory Syndrome of Jervell and Lange-Nielsen (Recessive Deafness with Electrocardiographic Abnormalities)

5. Pathology of the Ear in the Cardio-Auditory Syndrome of Jervell and Lange-Nielsen

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