Congenital monocular elevation deficiency associated with a novel TUBB3 gene variant. (2020)
Attributed to:
Optical coherence tomography in infants and children: A normative database and assessment of clinical use
funded by
MRC
Abstract
No abstract provided
Bibliographic Information
Digital Object Identifier: http://dx.doi.org/10.1136/bjophthalmol-2019-314293
PubMed Identifier: 31302631
Publication URI: http://europepmc.org/abstract/MED/31302631
Type: Journal Article/Review
Volume: 104
Parent Publication: The British journal of ophthalmology
Issue: 4
ISSN: 0007-1161