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Determining immune components necessary for progression of pigment dispersing disease to glaucoma in DBA/2J mice
BACKGROUND: The molecular mechanisms causing pigment dispersion syndrome (PDS) and the pathway(s) by which it progresses to pigmentary glaucoma are not known. Mutations in two melanosomal protein genes (Tyrp1( b ) and Gpnmb( R150X )) are responsible for pigment dispersing iris disease, which progres...
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| Huvudupphovsmän: | , , , , |
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| Materialtyp: | Artigo |
| Språk: | Inglês |
| Publicerad: |
BioMed Central
2014
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| Ämnen: | |
| Länkar: | https://ncbi.nlm.nih.gov/pmc/articles/PMC3974199/ https://ncbi.nlm.nih.gov/pubmed/24678736 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1186/1471-2156-15-42 |
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