DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Andelfinger G, Tapper AR, Welch RC, Vanoye CG, George Jr AL, Benson DW.
KCNJ2 mutation results in Andersen syndrome with sex-specific cardiac and skeletal muscle phenotypes.
Am J Hum Genet 2002;
71 (03) 663-668
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