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The predisposition to thyrotoxic periodic paralysis (TPP) is due to a genetic variant in the inward-rectifying potassium channel, KCNJ2.

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Title: The predisposition to thyrotoxic periodic paralysis (TPP) is due to a genetic variant in the inward-rectifying potassium channel, KCNJ2.
Authors: Wang X; Department of Chemical Pathology, The Chinese University of Hong Kong, N.T., Hong Kong SAR; Functional Genomics and Biostatistical Computing Laboratory, Shenzhen Research Institute of the Chinese University of Hong Kong., Chow CC, Yao X, Ko GT, Cockram CS, Kwok HK, Zhang J, Tang NL
Source: Clinical endocrinology [Clin Endocrinol (Oxf)] 2014 May; Vol. 80 (5), pp. 770-1. Date of Electronic Publication: 2013 Jul 31.
Publication Type: Letter
Journal Info: Publisher: Blackwell Publishing Country of Publication: England NLM ID: 0346653 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1365-2265 (Electronic) Linking ISSN: 03000664 NLM ISO Abbreviation: Clin Endocrinol (Oxf) Subsets: MEDLINE
Database: MEDLINE Ultimate
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ISSN:1365-2265
DOI:10.1111/cen.12277