Pathophysiological Mechanisms of Dominant and Recessive KvLQT1 K+ Channel Mutations Found in Inherited Cardiac Arrhythmias

By Wollnik Bernd  

Human Molecular Genetics, Vol. 6, Iss. 11, 1997-10 ,pp. : 1943-1949

Oxford University Press

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LIT1 , an imprinted antisense RNA in the human KvLQT1 locus identified by screening for differentially expressed transcripts using monochromosomal hybrids

By Mitsuya Kohzoh  

Human Molecular Genetics, Vol. 8, Iss. 7, 1999-07 ,pp. : 1209-1217

Oxford University Press

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KVLQT1 Mutations in Three Families with Familial or Sporadic Long QT Syndrome

By Russell Mark W.   Dick Macdonald   Collins Francis S.   Brody Lawrence C.  

Human Molecular Genetics, Vol. 5, Iss. 9, 1996-01 ,pp. : 1319-1324

Oxford University Press

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Mutations in the Gene Encoding the Inwardly-Rectifying Renal Potassium Channel, ROMK, Cause the Antenatal Variant of Bartter Syndrome: Evidence for Genetic Heterogeneity

By Károlyi Lothar  

Human Molecular Genetics, Vol. 6, Iss. 1, 1997-01 ,pp. : 17-26

Oxford University Press

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Cellular dysfunction of LQT5-minK mutants: abnormalities of I Ks , I Kr and trafficking in long QT syndrome

By Bianchi Laura  

Human Molecular Genetics, Vol. 8, Iss. 8, 1999-08 ,pp. : 1499-1507

Oxford University Press

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