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Ocular congenital cranial dysinnervation disorders (CCDDs): insights into axon growth and guidance
Unraveling the genetics of the paralytic strabismus syndromes known as congenital cranial dysinnervation disorders (CCDDs) is both informing physicians and their patients and broadening our understanding of development of the ocular motor system. Genetic mutations underlying ocular CCDDs alter eithe...
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| Gepubliceerd in: | Hum Mol Genet |
|---|---|
| Hoofdauteurs: | , |
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2017
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| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC5886468/ https://ncbi.nlm.nih.gov/pubmed/28459979 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddx168 |
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