Lattice corneal dystrophy, gelsolin type (Meretojaâs syndrome)
Author:
Publisher
Wiley
Subject
Ophthalmology,General Medicine
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1755-3768.2009.01686.x/fullpdf
Reference31 articles.
1. Reply to âArdalan Shoja Kiuru syndrome hereditary gelsolin amyloidosis plus retinitis pigmentosaâ;Ardalan;Nephrol Dial Transplant,2007
2. Amyloidosis-related nephrotic syndrome due to a G654A gelsolin mutation: the first report from the Middle East;Ardalan;Nephrol Dial Transplant,2007
3. Cardiac conduction alterations in a French family with amyloidosis of the Finnish type with the p.Asp187Tyr mutation in the GSN gene;Chastan;Muscle Nerve,2006
4. Gelsolin-related familial amyloidosis, Finnish type, in a Portuguese family: clinical and neurophysiological studies;Conceicao;Muscle Nerve,2003
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