Response to Weisschuh's "Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype".
Mano, Fukutaro
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
Publication Type: Journal Article; Comment
1744-5094
10.1080/13816810.2018.1558264 doi
Bestrophins
Choroid Diseases
Eye Diseases, Hereditary
Humans
Mutation, Missense
Phenotype
Retinal Degeneration
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
Publication Type: Journal Article; Comment
1744-5094
10.1080/13816810.2018.1558264 doi
Bestrophins
Choroid Diseases
Eye Diseases, Hereditary
Humans
Mutation, Missense
Phenotype
Retinal Degeneration