Novel WT1 Missense Mutations in Han Chinese Women with Premature Ovarian Failure
Author:
Publisher
Springer Science and Business Media LLC
Subject
Multidisciplinary
Link
http://www.nature.com/articles/srep13983.pdf
Reference29 articles.
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3. van Kasteren, Y. M. et al. Familial idiopathic premature ovarian failure: an overrated and underestimated genetic disease? Hum Reprod 14, 2455–2459 (1999).
4. Kuo, F. T., Bentsi-Barnes, I. K., Barlow, G. M. & Pisarska, M. D. Mutant Forkhead L2 (FOXL2) proteins associated with premature ovarian failure (POF) dimerize with wild-type FOXL2, leading to altered regulation of genes associated with granulosa cell differentiation. Endocrinology 152, 3917–3929, 10.1210/en.2010-0989 (2011).
5. Mansouri, M. R. et al. Alterations in the expression, structure and function of progesterone receptor membrane component-1 (PGRMC1) in premature ovarian failure. Human molecular genetics 17, 3776–3783, 10.1093/hmg/ddn274 (2008).
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