Genetic testing for infantile nystagmus
We studied the scientific literature and disease guidelines in order to summarize the clinical utility of genetic testing for infantile nystagmus (IN). Forms of IN associated with variations in CACNA1F, FRMD7 and GPR143 genes have X-linked recessive inheritance, whereas variations in SLC38A8, TYR an...
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| Principais autores: | , , , , , |
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| Format: | Artigo |
| Sprog: | Inglês |
| Udgivet: |
Sciendo
2017-10-01
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| Serier: | The EuroBiotech Journal |
| Online adgang: | https://doi.org/10.24190/ISSN2564-615X/2017/S1.18 |
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