Functional and clinical characterization of a mutation in KCNJ2 associated with Andersen-Tawil syndrome.

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Published in J Med Genet on March 29, 2006

Authors

C-W Lu1, J-H Lin, Y S Rajawat, H Jerng, T G Rami, X Sanchez, G DeFreitas, B Carabello, F DeMayo, D L Kearney, G Miller, H Li, P J Pfaffinger, N E Bowles, D S Khoury, J A Towbin

Author Affiliations

1: Department of Pediatrics, Shin Kong Wu Ho-Su Memorial Hospital, Taipei, Taiwan.

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