Retinal Avascularity and Neovascularization Associated With LAMA1 (laminin1) Mutation in Poretti-Boltshauser Syndrome. uri icon

Overview

publication date

  • January 1, 2018

Research

keywords

  • Abnormalities, Multiple
  • Apraxias
  • Cogan Syndrome
  • Intellectual Disability
  • Laminin
  • Mutation
  • Retinal Neovascularization
  • Retinal Vessels

Identity

Scopus Document Identifier

  • 85041129078

Digital Object Identifier (DOI)

  • 10.1001/jamaophthalmol.2017.5060

PubMed ID

  • 29167897

Additional Document Info

volume

  • 136

issue

  • 1