Skip Navigation



Hum. Reprod. Advance Access published online on May 16, 2008
Human Reproduction, doi:10.1093/humrep/den063
This Article
Right arrow Full Text
Right arrow Full Text (PDF )
Right arrow Submit a response
Right arrow Alert me when this article is cited
Right arrow Alert me when eLetters are posted
Right arrow Alert me if a correction is posted
Services
Right arrow Email this article to a friend
Right arrow Similar articles in this journal
Right arrow Similar articles in PubMed
Right arrow Alert me to new issues of the journal
Right arrow Add to My Personal Archive
Right arrow Download to citation manager
Right arrowRequest Permissions
Google Scholar
Right arrow Articles by Tsai-Morris, C.-H.
Right arrow Articles by Dufau, M. L.
PubMed
Right arrow PubMed Citation
Right arrow Articles by Tsai-Morris, C.-H.
Right arrow Articles by Dufau, M. L.
Social Bookmarking
Add to CiteULike   Add to Connotea   Add to Del.icio.us  
What's this?

Published by Oxford University Press on behalf of the European Society of Human Reproduction and Embryology 2008

Letter to the Editor

Differences in gonadotropin-regulated testicular helicase (GRTH/DDX25) single nucleotide polymorphism between Japanese and Chinese populations

Chon-Hwa Tsai-Morris1,3, Eitetsu Koh2 and Maria L. Dufau1

1 Section on Molecular Endocrinology, Endocrinology and Reproduction Research Branch, Program on Developmental Endocrinology and Genetics, National Institute of Child Health and Human Development, National Institute of Health, Bethesda, MD 20892, USA 2 Department of Urology, Kanazawa University School of Medicine, Ishikawa, Japan

3 Correspondence address. E-mail: morrisch@mail.nih.gov

The first 10% of the full text of this article appears below.

Sir,

We would like to make a comment on the article by Zhoucun et al. (2006)Go published in Human Reproduction, entitled ‘Single nucleotide polymorphisms of the gonadotropin-regulated testicular helicase (GRTH) gene may be associated with the human spermatogenesis impairment’. This specifically relates to the conclusion about their finding that allele T of c.852C -> T polymorphism of the GRTH gene might increase the risk of impaired spermatogenesis in humans. In contrast to their patient group . . . [Full Text of this Article]


Add to CiteULike CiteULike   Add to Connotea Connotea   Add to Del.icio.us Del.icio.us    What's this?