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Elsevier, Gene, (897), p. 148076, 2024

DOI: 10.1016/j.gene.2023.148076

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Functional and clinical characterization of a novel homozygous KCNH2 missense variant in the pore region of Kv11.1 leading to a viable but severe long-QT syndrome

This paper was not found in any repository, but could be made available legally by the author.
This paper was not found in any repository, but could be made available legally by the author.

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