Novel paraoxonase (PON1) nonsense and missense mutations predicted by functional genomic assay of PON1 status

Ovid Technologies (Wolters Kluwer Health) - Tập 13 Số 5 - Trang 291-295 - 2003
Gail P. Jarvik1,2,3, Rachel L. Jampsa1,2, Rebecca J. Richter1,2, Chris Carlson1,2, Mark J. Rieder1,2, Deborah A. Nickerson1,2, Clement E. Furlong1,2
1G.P.J), with additional funding from NIH P30ESO7033, PO1ES09601, EPA-R 826886-01-0, and NIH ES09883 and the Program for Genomic Applications (PGA) NIH-NHLBI U01 HL66682 and U01 HL6642.
2Sponsorship: This work was funded by the National Institutes of Health HL67406 and the Veteran Affairs Epidemiology Research and Information Centre Program (award CSP 701S
3requests for reprints to Gail Jarvik, University of Washington Medical Center, Division of Medical Genetics, Box 357720, Seattle, WA 98195-7720, USA.

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Ovid Technologies (Wolters Kluwer Health)

Tập 13 Số 5

291-295

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