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  • e0020 Compound heterozygous novel splicing mutation D202sp and missence mutation G272D on KCNQ1 caused Jervel and Lange-Nielsen syndrome in a Chinese family

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GWICC Abstracts 2010
Basic science: Cardiovascular disease basic research
e0020 Compound heterozygous novel splicing mutation D202sp and missence mutation G272D on KCNQ1 caused Jervel and Lange-Nielsen syndrome in a Chinese family
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Cite this article as:
Cuilan L, Wenling L, Ruijuan L, et al
e0020 Compound heterozygous novel splicing mutation D202sp and missence mutation G272D on KCNQ1 caused Jervel and Lange-Nielsen syndrome in a Chinese family
Heart 2010;96:A7.