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)

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10.1080/13816810.2018.1558264

Cite this

Response to Weisschuh’s “Comment : a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”. / Mano, Fukutaro; Pfannkoch, Cynthia; LoBue, Stephen A.; Olsen, Timothy ; Marmorstein, Alan D; Pulido, Jose S.

In: Ophthalmic Genetics, 01.01.2019.

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

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doi = "10.1080/13816810.2018.1558264",

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AU - Olsen, Timothy

AU - Marmorstein, Alan D

AU - Pulido, Jose S

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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

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