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 W. Olsen, Alan D Marmorstein, Jose S Pulido

Research output: Contribution to journalArticle

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 W.; Marmorstein, Alan D; Pulido, Jose S.

In: Ophthalmic Genetics, 01.01.2019.

Research output: Contribution to journalArticle

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