A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency-Reference-Cited by-同舟云学术

A novel heterozygous splice-altering mutation in HFM1 may be a cause of premature ovarian insufficiency

Published:2019-07-06 Issue:1 Volume:12 Page:
ISSN:1757-2215
Container-title:Journal of Ovarian Research
language:en
Short-container-title:J Ovarian Res

Author:

Zhe Jing,Chen Shiling,Chen Xin,Liu Yudong,Li Ying,Zhou Xingyu,Zhang Jun

Funder

the National Key Research & Developmental Program of China

the Clinical Research Startup Program of Southern Medical University by High-level University Construction Funding of Guangdong Provincial Department of Education

Clinical Research Program of Nanfang Hospital, Southern Medical University

Publisher

Springer Science and Business Media LLC

Subject

Obstetrics and Gynecology,Oncology

Link

http://link.springer.com/content/pdf/10.1186/s13048-019-0537-x.pdf

Reference24 articles.

1. Webber L, Davies M, Anderson R, Bartlett J, Braat D, Cartwright B, et al. ESHRE guideline: management of women with premature ovarian insufficiency. Hum Reprod. 2016;31:926–37.

2. Jiao X, Zhang H, Ke H, Zhang J, Cheng L, Liu Y, et al. Premature ovarian insufficiency: phenotypic characterization within different etiologies. J Clin Endocrinol Metab. 2017;102:2281–90.

3. Panay N. Management of premenstrual syndrome. J Fam Plann Reprod Health Care. 2009;35:187–94.

4. De Vos M, Devroey P, Fauser BC. Primary ovarian insufficiency. Lancet. 2010;376:911–21.

5. Nelson LM. Clinical practice. Primary ovarian insufficiency. N Engl J Med. 2009;360:606–14.

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