FSH-RF |
FSH suppressing protein |
integrin-beta-2 |
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[FSH-resistant ovaries] This term pertains to a 566C-->T mutation in the FSHR [follicle-stimulating hormone receptor; FSH receptor], which causes ovarian dysgenesis, characterized by primary or early secondary amenorrhea, variable development of secondary sex characteristics, and high serum levels of FSH [Follicle-stimulating hormone] and Luteinizing hormone. (Aittomäki et al, 1996). The locus is being referred to also as ODG1 [Ovarian Dysgenesis 1].
See also: hormones/neuropeptide MiniCOPE dictionary for hormonally active proteins, peptides, neuropeptides, regulatory peptides,
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