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Citation: At. Remaley et al., Human ATP-binding cassette transporter 1 (ABC1): Genomic organization and identification of the genetic defect in the original Tangier disease kindred, P NAS US, 96(22), 1999, pp. 12685-12690
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Tahvanainen, E
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Funke, H
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Authors:
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Denjoy, I
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Hammoude, H
Klug, D
Schulze-Bahr, E
Richard, P
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Schwartz, K
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Citation: M. Berthet et al., C-terminal HERG mutations - The role of hypokalemia and a KCNQ1-associatedmutation in cardiac event occurrence, CIRCULATION, 99(11), 1999, pp. 1464-1470