Mano, Fukutaro <br/><br/>
Response to Weisschuh's "Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype".  [electronic resource] 

 -  Ophthalmic genetics  02 2019 
 - 88-89 p.  digital 
<br/><br/> Publication Type: Journal Article; Comment 
<br/><br/><label>ISSN: </label>1744-5094 
<br/><br/><label>Standard No.: </label>10.1080/13816810.2018.1558264  doi 
<br/><br/><label>Subjects--Topical Terms: </label><br/>Bestrophins<br/>Choroid Diseases<br/>Eye Diseases, Hereditary<br/>Humans<br/>Mutation, Missense<br/>Phenotype<br/>Retinal Degeneration