Genetic testing for color vision deficiency
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of genetic testing for color vision deficiency (CVD). Deuteranopia affects 1 in 12 males and is inherited in an X-linked recessive manner. It is associated with variations in the OPN1LW (OMIM gene:...
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| Principais autores: | , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado: |
Sciendo
2017-10-01
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| Series: | The EuroBiotech Journal |
| Acceso en liña: | https://doi.org/10.24190/ISSN2564-615X/2017/S1.10 |
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