Response to Weisschuh’s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”

Fukutaro Mano; Cynthia Pfannkoch; Stephen A. LoBue; Timothy Olsen; Alan D Marmorstein; Jose S Pulido

doi:10.1080/13816810.2018.1558264

Response to Weisschuh’s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”

Fukutaro Mano, Cynthia Pfannkoch, Stephen A. LoBue, Timothy Olsen, Alan D Marmorstein, Jose S Pulido

Ophthalmology

Research output: Contribution to journal › Article › peer-review

Original language	English (US)
Journal	Ophthalmic Genetics
DOIs	https://doi.org/10.1080/13816810.2018.1558264
State	Accepted/In press - Jan 1 2019

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health
Ophthalmology
Genetics(clinical)

Access to Document

10.1080/13816810.2018.1558264

Cite this

@article{57475dae7e66492ba086f1e281db2c1a,

title = "Response to Weisschuh{\textquoteright}s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”",

author = "Fukutaro Mano and Cynthia Pfannkoch and LoBue, {Stephen A.} and Timothy Olsen and Marmorstein, {Alan D} and Pulido, {Jose S}",

year = "2019",

month = jan,

day = "1",

doi = "10.1080/13816810.2018.1558264",

language = "English (US)",

journal = "Ophthalmic Genetics",

issn = "1381-6810",

publisher = "Informa Healthcare",

}

TY - JOUR

T1 - Response to Weisschuh’s “Comment

T2 - a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”

AU - Mano, Fukutaro

AU - Pfannkoch, Cynthia

AU - LoBue, Stephen A.

AU - Olsen, Timothy

AU - Marmorstein, Alan D

AU - Pulido, Jose S

PY - 2019/1/1

Y1 - 2019/1/1

UR - http://www.scopus.com/inward/record.url?scp=85059947683&partnerID=8YFLogxK

UR - http://www.scopus.com/inward/citedby.url?scp=85059947683&partnerID=8YFLogxK

U2 - 10.1080/13816810.2018.1558264

DO - 10.1080/13816810.2018.1558264

M3 - Article

C2 - 30632873

AN - SCOPUS:85059947683

JO - Ophthalmic Genetics

JF - Ophthalmic Genetics

SN - 1381-6810

ER -

Response to Weisschuh’s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”

ASJC Scopus subject areas

Access to Document

Other files and links

Cite this