MeSH(Medical Subject Headings) 맞춤 검색 (http://www.nlm.nih.gov) 결과 : 1 페이지: 1
Andersen Syndrome - 새창
A clinical triad consisting of potassium-sensitive periodic paralysis, ventricular ectopy, and dysmorphic features. It results from mutations in the KCNJ2 gene which codes for the INWARD RECTIFIER POTASSIUM CHANNELS subfamily J, member 2 (KCNJ2 protein, human.)
Synonyms : Long QT Syndrome 7, Syndrome, Andersen
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MeSH(Medical Subject Headings) 유사 검색 (http://www.nlm.nih.gov) 결과 : 0 페이지: 1
