DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Chan HF, Chen ML, Su JJ, Ko LC, Lin CH, Wu RM.
A novel neuropsychiatric phenotype of KCNJ2 mutation in one Taiwanese family with Andersen-Tawil syndrome.
J Hum Genet 2010;
55 (03) 186-188
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