Bonnin, N <br/><br/>
[Meretoja syndrome: Identification of a family and description of the corneal involvement by confocal microscopy].  [electronic resource] 

 -  Journal francais d'ophtalmologie  Jun 2015 
 - e111-5 p.  digital 
<br/><br/> Publication Type: Case Reports; Letter 
<br/><br/><label>ISSN: </label>1773-0597 
<br/><br/><label>Standard No.: </label>10.1016/j.jfo.2014.10.016  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Aged<br/>Amyloidosis--diagnosis<br/>Chromosome Aberrations<br/>Cornea--pathology<br/>Corneal Dystrophies, Hereditary--diagnosis<br/>DNA Mutational Analysis<br/>Diagnosis, Differential<br/>Gelsolin--genetics<br/>Genes, Dominant--genetics<br/>Humans<br/>Male<br/>Microscopy, Confocal<br/>Pedigree<br/>Rare Diseases