| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 6180821 | Fertility and Sterility | 2011 | 6 Pages |
Abstract
We describe a genetic basis for EFS and provide strong evidence for the existence of genuine EFS in some patients. A mutation impairing the function of LHCGR explains the lack of response of these patients to repeated administration of β-hCG.
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Authors
Kemal O. Ph.D., Tom Ph.D., Asli M.D., Michail M.D., Duygu Ph.D., Gogsen M.D., Mary-Claire Ph.D., Mustafa M.D.,