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In a paper published in the journal Science
scientists from deCODE genetics (Nasdaq CGN) and academic colleagues from the National University Hospital in Reykjavik and Uppsala University in Sweden report the discovery of two common single letter variations (SNPs) in the sequence of the human genome that appear to account for virtually all cases of a major subtype of glaucoma. [click link for aaaa article]Linkleri Üyelerimiz Görebilir. UslanmaM Üyeliği İçin Tıklayın |
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