Results
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37141.
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37142.
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37143.
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Analysis of the human KCNH2(HERG) gene: identification and characterization of a novel mutation Y667X associated with long QT syndrome and a non-pathological 9 bp insertion. [electronic resource] by
- Paulussen, A
- Yang, P
- Pangalos, M
- Verhasselt, P
- Marrannes, R
- Verfaille, C
- Vandenberk, I
- Crabbe, R
- Konings, F
- Luyten, W
- Armstrong, M
Producer: 20000921
In:
Human mutation vol. 15
Availability: No items available.
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37144.
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37145.
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37146.
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37147.
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37148.
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37149.
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37150.
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37151.
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37152.
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37153.
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37154.
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37155.
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37156.
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37157.
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37158.
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37159.
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37160.
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