A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.

doi:10.1038/jhg.2012.20

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Article

A genome-wide association study identifies novel susceptibility genetic variation for thyrotoxic hypokalemic periodic paralysis.

Journal of human genetics - 1 May 2012

Jongjaroenprasert Wallaya, Phusantisampan Theerawut, Mahasirimongkol Surakameth, Mushiroda Taisei, Hirankarn Nattiya, Snabboon Thiti, Chanprasertyotin Suwannee, Tantiwong Puntip, Soonthornpun Supamai, Rattanapichart Paninee, Mamanasiri Sunee, Himathongkam Thep, Ongphiphadhanakul Boonsong, Takahashi Atsushi, Kamatani Naoyuki, Kubo Michiaki, Nakamura Yusuke

Abstract excerpt

Several lines of evidence have pointed out that genetic components have roles in thyrotoxic hypokalemic periodic paralysis (TTPP). In this study, for the first time we performed genome-wide association study (GWAS) in male hyperthyroid subjects in order to identify genetic loci conferring susceptibility to TTPP. We genotyped 78 Thai male TTPP cases and 74 Thai male hyperthyroid patients without hypokalemia as...

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PMID: 22399142
DOI: 10.1038/jhg.2012.20

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KCNJ2

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