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CYP1B1 mutations in French patients with early-onset primary open-angle glaucoma
Introduction: Primary open-angle glaucoma (POAG) is a leading cause of visual impairment worldwide and a complex genetic disorder that affects mostly adults. Mutations in the MYOCILIN (MYOC) and OPTINEURIN genes account for rare forms with a Mendelian inheritance and for <5% of all POAG cases. Th...
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| Main Authors: | , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
BMJ Group
2004
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| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1735887/ https://ncbi.nlm.nih.gov/pubmed/15342693 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/jmg.2004.020024 |
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