Wordt geladen...
Suppression of Ca(2+) signaling in a mouse model of Best disease
Mutations in BEST1, encoding bestrophin-1 (Best1), cause Best vitelliform macular dystrophy (BVMD), a dominantly inherited macular degeneration characterized by a diminished electrooculogram light peak (LP), lipofuscin in retinal pigment epithelial cells (RPE), and fluid- and debris-filled retinal d...
Bewaard in:
| Hoofdauteurs: | , , , , , , , |
|---|---|
| Formaat: | Artigo |
| Taal: | Inglês |
| Gepubliceerd in: |
Oxford University Press
2010
|
| Onderwerpen: | |
| Online toegang: | https://ncbi.nlm.nih.gov/pmc/articles/PMC2830833/ https://ncbi.nlm.nih.gov/pubmed/20053664 https://ncbi.nlm.nih.govhttp://dx.doi.org/10.1093/hmg/ddp583 |
| Tags: |
Voeg label toe
Geen labels, Wees de eerste die dit record labelt!
|