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Leber's congenital amaurosis (LCA) is a group of inherited blinding diseases with onset during childhood. One form of the disease, LCA2, is caused by mutations in the retinal pigment epithelium-specific ...
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Early-onset, severe retinal dystrophy caused by mutations in the gene encoding retinal pigment epithelium-specific 65-kDa protein (RPE65) is associated with poor vision at birth and complete loss of vision in ...
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(No abstract is available for this citation)
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Background There is an urgent need to determine whether oversulfated chondroitin sulfate (OSCS), a compound contaminating heparin supplies worldwide, is the cause of the severe anaphylactoid reactions that have occurred ...
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(No abstract is available for this citation)
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(No abstract is available for this citation)
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