Novel NOBOX loss-of-function mutations account for 6.2% of cases in a large primary ovarian insufficiency cohort. [electronic resource]
Producer: 20120117Description: 1108-13 p. digitalISSN:- 1098-1004
- Alleles
- Amino Acid Sequence
- Base Sequence
- Cohort Studies
- Female
- Gene Frequency
- Gene Order
- HEK293 Cells
- Heterozygote
- Homeodomain Proteins -- genetics
- Humans
- Models, Molecular
- Molecular Sequence Data
- Mutation
- Prevalence
- Primary Ovarian Insufficiency -- epidemiology
- Protein Conformation
- Sequence Alignment
- Transcription Factors -- genetics
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Publication Type: Journal Article; Research Support, Non-U.S. Gov't
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