Hereditary haemochromatosis gene (HFE) H63D mutation shows an association with abnormal sperm motility

Molecular Biology Reports

Volumn 36, Issue 7, 2009, Pages 1709-1714

  Gunel Ozcan, Aysen ^a,b   Basar, M Murad ^a   Kısa, Ucler ^a   Ankaralı, Handan C ^c  

^a KIRIKKALE UNIVERSITY   (Turkey)

^b HACETTEPE UNIVERSITY   (Turkey)

^c ZONGULDAK KARAELMAS UNIVERSITY   (Turkey)

Author keywords

H63D mutation; HFE; Infertility

Indexed keywords

FOLLITROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

ADOLESCENT; ADULT; ARTICLE; FOLLITROPIN BLOOD LEVEL; GENE; GENE FREQUENCY; GENE MUTATION; HEMOCHROMATOSIS; HFE GENE; HUMAN; LUTEINIZING HORMONE BLOOD LEVEL; MAJOR CLINICAL STUDY; MALE; MALE INFERTILITY; PATIENT SELECTION; SEMEN ABNORMALITY; SPERMATOZOON MOTILITY; TESTIS SIZE; TESTOSTERONE BLOOD LEVEL;

EID: 68149150519     PISSN: 03014851     EISSN: 15734978     Source Type: Journal    
DOI: 10.1007/s11033-008-9372-7     Document Type: Article

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