| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 3932411 | Fertility and Sterility | 2011 | 14 Pages |
Abstract
Given their putative effect on protein structure, their location in conserved sequences or functional domains, and their absence in controls, the identified mutations may be a cause of asthenozoospermia in humans.
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Authors
Liesbeth M.D., M.Sc., G. Henrike M.D., Ph.D., Fang Ph.D., Saskia K.M. B.Sc., Fulco M.D., Ph.D., M. Paola Ph.D., Sjoerd Ph.D.,