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Coexistence of macular corneal dystrophy types I and II in a single sibship

BACKGROUND—Macular corneal dystrophy (MCD) is an inherited autosomal recessive disorder that has been subdivided into two primary immunophenotypes, MCD types I and II. The MCD type I gene has been localised previously to chromosome 16q22 and suggestive evidence provided that MCD type II gene is also...

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Autors principals: Liu, N., Baldwin, J., Lennon, F., Stajich, J., Thonar, E., Pericak-Vance, M., Klintworth, G., Vance, J.
Format: Artigo
Idioma:Inglês
Publicat: 1998
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Accés en línia:https://ncbi.nlm.nih.gov/pmc/articles/PMC1722518/
https://ncbi.nlm.nih.gov/pubmed/9602619
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