Mutations in HFM1 in recessive primary ovarian insufficiency

N Engl J Med. 2014 Mar 6;370(10):972-4. doi: 10.1056/NEJMc1310150.

Authors

Jian Wang¹, Wenxiang Zhang, Hong Jiang, Bai-Lin Wu; Primary Ovarian Insufficiency Collaboration

Collaborators

Primary Ovarian Insufficiency Collaboration:
Bai-Lin Wu, Yu An, Bingbing Wu, Li Yu, Wenhao Zhou, Hong Jiang, Wenxiang Zhang, Xiaomin Song, Wenxiang Zhang, Hong Jiang, Jie Wu, Danhua Pu, Min Zhang, Bai-Lin Wu, Yiping Shen, Bai-Lin Wu, Jian Wang, Wenxiang Zhang, Yiping Shen, Chang Lin, Leslie Grimmett, Eileen Liao, Hong Shao, Xiaoming Shen, Orah Platt

Affiliation

¹ Boston Children's Hospital, Boston, MA.

PMID: 24597873
DOI: 10.1056/NEJMc1310150

No abstract available

Publication types

Letter
Research Support, Non-U.S. Gov't

MeSH terms

Amino Acid Sequence
DNA Helicases / genetics*
Female
Genes, Recessive
Heterozygote
Humans
Meiosis / genetics
Molecular Sequence Data
Mutation*
Primary Ovarian Insufficiency / genetics*

Substances

HFM1 protein, human
DNA Helicases