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Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation.

Deeb R, Veerapandiyan A, Tawil R, Treidler S. Variable penetrance of Andersen-Tawil syndrome in a family with a rare missense KCNJ2 mutation. Neurol Genet. 2018 Dec; 4(6):e284.

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