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Choline Dehydrogenase Polymorphism rs12676 Is a Functional Variation and Is Associated with Changes in Human Sperm Cell Function

Approximately 15% of couples are affected by infertility and up to half of these cases arise from male factor infertility. Unidentified genetic aberrations such as chromosomal deletions, translocations and single nucleotide polymorphisms (SNPs) may be the underlying cause of many cases of idiopathic...

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Detalles Bibliográficos
Autores principales: Johnson, Amy R., Lao, Sai, Wang, Tongwen, Galanko, Joseph A., Zeisel, Steven H.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3338626/
https://www.ncbi.nlm.nih.gov/pubmed/22558321
http://dx.doi.org/10.1371/journal.pone.0036047

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