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PITX3 mutations associated with autosomal dominant congenital cataract in the Chinese population
The present study aimed to identify the disease-causing gene of a four-generation Chinese family affected with congenital posterior subcapsular cataracts (CPSC), to additionally investigate the frequency of paired like homeodomain 3 (PITX3) mutations in Chinese patients with autosomal dominant conge...
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| 出版年: | Mol Med Rep |
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| 主要な著者: | , , , , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
D.A. Spandidos
2019
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6423573/ https://ncbi.nlm.nih.gov/pubmed/30816539 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.3892/mmr.2019.9989 |
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