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OLFM2
Gene Information from Publications |
| Publication Link |
Summary of findings |
| 17122126 |
Observational study of gene-disease association and gene-gene interaction. (HuGE Navigator) |
| 17122126 |
The Arg144Gln mutation in OLFM2 is a possible disease-causing mutation in Japanese patients with OAG. Common polymorphisms in OLFM2 and OPTN may interactively contribute to the development of OAG, indicating a polygenic etiology. |
OLFM2 results (if any) from reagent suppliers |
| Search Bioportfolio and other Life Science Sites for OLFM2,
or search for OLFM2 on BioPortfolio's antibody search engine. This page has been viewed 72 times Resources from the NCBI used on this page, NCBI's standard disclaimer applies.
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