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Exome sequencing identifies a novel UNC5D mutation in a severe myopic anisometropia family: A case report
INTRODUCTION: Severe myopic anisometropia has been identified to have heritability, but the pathogenesis of anisometropia still remains obscure. CASE DESCRIPTION: Here, we presented a Chinese severe myopic anisometropia family with 5 members affected. Though using the exome sequencing, we identified...
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| Veröffentlicht in: | Medicine (Baltimore) |
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| Hauptverfasser: | , , , , , |
| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Wolters Kluwer Health
2017
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| Schlagworte: | |
| Online Zugang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5478323/ https://ncbi.nlm.nih.gov/pubmed/28614238 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1097/MD.0000000000007138 |
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