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Authors: SCHULZEBAHR E HAVERKAMP W WEDEKIND H RUBIE C HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H

Citation: E. Schulzebahr et al., AUTOSOMAL RECESSIVE LONG-QT SYNDROME (JERVELL LANGE-NIELSEN SYNDROME)IS GENETICALLY HETEROGENEOUS, Human genetics, 100(5-6), 1997, pp. 573-576

Authors: SCHULZEBAHR E WANG Q HAVERKAMP W WEDEKIND H RUBIE C CHEN QY HORDT M BREITHARDT G FUNKE H

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Citation: E. Schulzebahr et al., IDENTIFICATION AND FUNCTIONAL-CHARACTERIZATION OF A NOVEL GENE FOR AUTOSOMAL RECESSIVE DEAFNESS AND LONG-QT SYNDROME (JERVELL AND LANGE-NIELSEN-SYNDROME), American journal of human genetics, 61(4), 1997, pp. 48-48

Authors: WEDEKIND H SCHULZEBAHR E LANGE S RUBIE C HAVERKAMP W HORDT M BORGGREFE M ASSMANN G BREITHARDT G FUNKE H

Citation: H. Wedekind et al., A SEVERE FORM OF LONG-QT SYNDROME CAUSED BY 2 KVLQT1 MUTATIONS LOCATED IN CIS, American journal of human genetics, 61(4), 1997, pp. 2051-2051