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A novel keratin 12 mutation in a German kindred with Meesmann's corneal dystrophy
AIM—To study a kindred with Meesmann's corneal dystrophy (MCD) to determine if a mutation within the cornea specific K3 or K12 genes is responsible for the disease phenotype. METHODS—Slit lamp examination of the cornea in four members of the kindred was carried out to confirm the diagnosis of M...
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| Main Authors: | , , , , , , |
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| Formato: | Artigo |
| Idioma: | Inglês |
| Publicado em: |
2000
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| Assuntos: | |
| Acesso em linha: | https://ncbi.nlm.nih.gov/pmc/articles/PMC1723457/ https://ncbi.nlm.nih.gov/pubmed/10781519 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1136/bjo.84.5.527 |
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