Sequence analysis of the X-linked USP26 gene in severe male factor infertility patients and fertile controls

Sequence analysis of the X-linked USP26 gene in severe male factor infertility patients and fertile controls

The 1090C>T,L364F variant of the ubiquitin protease 26 (USP26) gene does not appear to be related to male infertility. Mutations of the USP26 gene do not appear to be a common cause of idiopathic azoospermia or severe oligozoospermia.

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Bibliographische Detailangaben
Veröffentlicht in:Fertility and sterility 2008-09, Vol.90 (3), p.851-852
Hauptverfasser: Christensen, Greg L., Ph.D, Griffin, Jeanine, Carrell, Douglas T., Ph.D
Format: Artikel
Sprache:eng
Schlagworte:
Biological and medical sciences
Birth control
Cysteine Endopeptidases - genetics
Fertility - genetics
Genes, X-Linked - genetics
Genetic Predisposition to Disease - epidemiology
Genetic Predisposition to Disease - genetics
Gynecology. Andrology. Obstetrics
Humans
Infertility, Male - epidemiology
Infertility, Male - genetics
Internal Medicine
Male
Medical sciences
Obstetrics and Gynecology
Prevalence
Risk Assessment - methods
Risk Factors
Sequence Analysis, DNA
Severity of Illness Index
Sterility. Assisted procreation
Utah - epidemiology
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Beschreibung
Zusammenfassung:The 1090C>T,L364F variant of the ubiquitin protease 26 (USP26) gene does not appear to be related to male infertility. Mutations of the USP26 gene do not appear to be a common cause of idiopathic azoospermia or severe oligozoospermia.
ISSN:0015-0282
1556-5653
DOI:10.1016/j.fertnstert.2007.06.096