Genetic testing for optic atrophy
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of the genetic test for optic atrophy (OA). OA is mostly inherited in an autosomal dominant manner, rarely in an autosomal recessive manner, with an overall prevalence of 3/100,000 live births. It...
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| Hauptverfasser: | , , , , , |
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| Format: | Artigo |
| Sprache: | Inglês |
| Veröffentlicht: |
Sciendo
2017-10-01
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| Schriftenreihe: | The EuroBiotech Journal |
| Online-Zugang: | https://doi.org/10.24190/ISSN2564-615X/2017/S1.26 |
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