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vitskapeleg artikkel artigo científico (publicado na 1995-02) mokslinis straipsnis vetenskaplig artikel (publicerad på 1995-02) 1995 nî lūn-bûn scientific article wetenschappelijk artikel (gepubliceerd op 1995-02) научни чланак наукова стаття, опублікована в лютому 1995 artículu científicu espublizáu en 1995 vedecký článok (publikovaný 1995-02) artikull shkencor 1995年论文 1995年論文 мақолаи илмӣ 1995 թուականի Փետրուարին հրատարակուած գիտական յօդուած bilimsel makale article científic 1995年論文 1995年论文 artigo científico (publicado na 1995) tieteellinen artikkeli vědecký článek publikovaný v roce 1995 научная статья scienca artikolo ১৯৯৫-এ প্রকাশিত বৈজ্ঞানিক নিবন্ধ บทความทางวิทยาศาสตร์ مقالة علمية (نشرت في فبراير 1995) bài báo khoa học tudományos cikk 1995年论文 1995年論文 1995 թվականի փետրվարին հրատարակված գիտական հոդված videnskabelig artikel (udgivet 1995-02) article scientific artykuł naukowy artikulong pang-agham teaduslik artikkel articolo scientifico (pubblicato il 1995-02) 1995년 논문 article scientifique (publié 1995-02) سائنسی مضمون wissenschaftlicher Artikel (veröffentlicht in 1995-02) artículo científico publicado en 1995 επιστημονικό άρθρο 1995年論文 1995年论文 1995年の論文 мақолаи илмӣ vitenskapelig artikkel artigo científico مقالهٔ علمی naučni članak 1995年论文 מאמר מדעי სამეცნიერო სტატია articol științific 1995年論文 научни чланак 1995年论文 научна статия
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Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
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Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
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Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
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Hypokalemic periodic paralysis and the dihydropyridine receptor (CACNL1A3): genotype/phenotype correlations for two predominant mutations and evidence for the absence of a founder effect in 16 caucasian families
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