A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract.
A novel mutation in the OAR domain of PITX3 associated with congenital posterior subcapsular cataract. — المؤلف: Fan, Qi — BMC medical genetics 20190820
- المؤلف
- Fan, Qi
- النشر
- BMC medical genetics 20190820
- الوصف
- 42 p.
- الموضوعات
- Cataract؛ Female؛ Genetic Association Studies؛ Genetic Predisposition to Disease؛ High-Throughput Nucleotide Sequencing؛ Homeodomain Proteins؛ Humans؛ Male