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Autor:
Zurab R Tsetskhladze, Victor A Canfield, Khai C Ang, Steven M Wentzel, Katherine P Reid, Arthur S Berg, Stephen L Johnson, Koichi Kawakami, Keith C Cheng
Publikováno v:
PLoS ONE, Vol 7, Iss 10, p e47398 (2012)
A major challenge in personalized medicine is the lack of a standard way to define the functional significance of the numerous nonsynonymous, single nucleotide coding variants that are present in each human individual. To begin to address this proble
Externí odkaz:
https://doaj.org/article/da3862002040408fb9a144dce163ab1c