Laser Clearance of Drusen Deposit in Patients With Autosomal Dominant Drusen (p.Arg345Trp in EFEMP1)

Author:

Lenassi Eva,Troeger Eric,Wilke Robert,Tufail Adnan,Hawlina Marko,Jeffery Glen,Webster Andrew R.

Publisher

Elsevier BV

Subject

Ophthalmology

Reference31 articles.

1. A peculiar condition of choroiditis occurring in several members of the same family;Doyne;Trans Ophthalmol Soc UK,1899

2. Die Ophthalmoskopie im rotfreien Licht;Vogt,1925

3. A novel haplotype with the R345W mutation in the EFEMP1 gene associated with autosomal dominant drusen in a Japanese family;Takeuchi;Invest Ophthalmol Vis Sci,2010

4. Maculopathy due to the R345W substitution in fibulin-3: distinct clinical features, disease variability, and extent of retinal dysfunction;Michaelides;Invest Ophthalmol Vis Sci,2006

5. A single EFEMP1 mutation associated with both Malattia Leventinese and Doyne honeycomb retinal dystrophy;Stone;Nat Genet,1999

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