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