A novel SRY mutation leads to asymmetric SOX9 activation and is responsible for mixed 46,XY gonadal dysgenesis.
2012
Background: SRY, located on the Y chromosome, is one of the key genes involved in human sex determination. SRY mutations are responsible for 10–15% of all cases o
Keywords:
- Correction
- Source
- Cite
- Save
- Machine Reading By IdeaReader
16
References
5
Citations
NaN
KQI