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Exome sequencing in families with chronic central serous chorioretinopathy
BACKGROUND: Central serous chorioretinopathy (CSC) is a chorioretinal disease characterized by fluid accumulation between the neuroretina and retinal pigment epithelium with unknown etiology. Family studies have suggested a heritable component for CSC with an autosomal dominant inheritance pattern....
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| 出版年: | Mol Genet Genomic Med |
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| 主要な著者: | , , , , , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
John Wiley and Sons Inc.
2019
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| 主題: | |
| オンライン・アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6465660/ https://ncbi.nlm.nih.gov/pubmed/30724488 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1002/mgg3.576 |
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