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

Research output: Contribution to journal › Article

Original languageEnglish (US)
JournalOphthalmic Genetics
DOIs
StateAccepted/In press - Jan 1 2019

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Missense Mutation
Phenotype
Vitreoretinochoroidopathy

ASJC Scopus subject areas

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

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

Mano, F, Pfannkoch, C, LoBue, SA, Olsen, T, Marmorstein, AD & Pulido, JS 2019, 'Response to Weisschuh’s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”', Ophthalmic Genetics. https://doi.org/10.1080/13816810.2018.1558264
Mano F, Pfannkoch C, LoBue SA, Olsen T, Marmorstein AD, Pulido JS. Response to Weisschuh’s “Comment: a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”. Ophthalmic Genetics. 2019 Jan 1. https://doi.org/10.1080/13816810.2018.1558264
Mano, Fukutaro ; Pfannkoch, Cynthia ; LoBue, Stephen A. ; Olsen, Timothy ; Marmorstein, Alan D ; Pulido, Jose S. / Response to Weisschuh’s “Comment : a novel missense mutation in BEST1 associated with an autosomal-dominant vitreoretinochoroidopathy (ADVIRC) phenotype”. In: Ophthalmic Genetics. 2019.
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