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Genotypes and phenotypes of genes associated with achromatopsia: A reference for clinical genetic testing
PURPOSE: Achromatopsia is a congenital autosomal recessive cone disorder, and it has been found to be associated with six genes. However, pathogenic variants in these six genes have been identified in patients with various retinal dystrophies with the exception of achromatopsia. Thus, this study aim...
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| 出版年: | Mol Vis |
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| 主要な著者: | , , , , |
| フォーマット: | Artigo |
| 言語: | Inglês |
| 出版事項: |
Molecular Vision
2020
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| 主題: | |
| オンライン･アクセス: | https://ncbi.nlm.nih.gov/pmc/articles/PMC7479066/ https://ncbi.nlm.nih.gov/pubmed/32913385 |
| タグ: |
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