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Prevalence of congenital colour vision deficiency among Black school children in Durban, South Africa
OBJECTIVES: Congenital colour vision deficiency (CCVD) is an x-linked chromosome disorder that results from abnormalities in one or all three-cone type’s photoreceptors. Early assessment and diagnosis of CCVD is necessary to minimise the disability associated with the condition. Multistage sampling...
Salvato in:
| Pubblicato in: | BMC Res Notes |
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| Autori principali: | , |
| Natura: | Artigo |
| Lingua: | Inglês |
| Pubblicazione: |
BioMed Central
2019
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| Soggetti: | |
| Accesso online: | https://ncbi.nlm.nih.gov/pmc/articles/PMC6558866/ https://ncbi.nlm.nih.gov/pubmed/31182158 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/s13104-019-4374-1 |
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