Title : Polymorphisms of SLC22A9 (hOAT7) in Korean Females with Osteoporosis.

Pub. Date : 2015 Jul

PMID : 26170735






1 Functional Relationships(s)
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1 The present study demonstrates that the SLC22A9 variant F426S is causing inter-individual variation that is leading to the differences in transport of the steroid sulfate conjugate (estrone sulfate) and, therefore this could be used as a marker for certain disease including osteoporosis. steroid sulfate solute carrier family 22 member 9 Homo sapiens