Genetic testing for cone rod dystrophies
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of the genetic test for cone rod dystrophies (CORDs). CORDs are caused by variations in the ABCA4, ADAM9, AIPL1, C8orf37, CACNA1F, CACNA2D4, CDHR1, CNGA3, CRX, DRAM2, GUCA1A, GUCY2D, HRG4, KCNV2, P...
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| Autors principals: | , , , , , |
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| Format: | Artigo |
| Idioma: | Inglês |
| Publicat: |
Sciendo
2017-10-01
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| Col·lecció: | The EuroBiotech Journal |
| Accés en línia: | https://doi.org/10.24190/ISSN2564-615X/2017/S1.11 |
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