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Targeted next-generation sequencing extends the mutational spectrums for OPA1 mutations in Chinese families with optic atrophy
PURPOSE: We aim to reveal the disease-causing mutations in 15 Chinese families with optic atrophy (OA). METHODS: In total, 15 families with OA were recruited in the present study. Medical histories were carefully reviewed and comprehensive ophthalmic examinations were received by all recruited patie...
Sparad:
| I publikationen: | Mol Vis |
|---|---|
| Huvudupphovsmän: | , , , , , , , , |
| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
Molecular Vision
2019
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6982427/ https://ncbi.nlm.nih.gov/pubmed/32025183 |
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