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On the Trail of a Point Mutation

About 4 pages (1,078 words)

The Scientist, November 1st, 2006

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William Vainchenker had long suspected a rogue JAK2 tyrosine kinase to be the cause of the myeloproliferative disorder, polycythemia vera. But with very limited resources at his disposal at the Gustave Roussy Institute in Paris, he could not afford large-scale sequencing efforts. Working with only three patients, his team concentrated on tracking down JAK2 gene mutations. "We were lucky," says Vainchenker. "We found the same mutation in two of them."

The culprit turned out to be a single nucleotide mutation at codo...

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Shekhar, Chandra. The Scientist, November 1st, 2006. On the Trail of a Point Mutation. Content provided by HighBeam Research.



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