Nanophthalmos: a systematic review of the clinical spectrum of nanophthalmos, its genetic basis, prevalence, incidence, clinical and surgical management
Author:
Publisher
Edizioni Minerva Medica
Subject
General Medicine
Link
https://www.minervamedica.it/pdf.php?cod=R12Y2019N03A0042
Reference102 articles.
1. High-hyperopia database, part I: clinical characterisation including morphometric (biometric) differentiation of posterior microphthalmos from nanophthalmos
2. Genetics of Refraction and Myopia
3. Genetic susceptibility and mechanisms for refractive error
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5. Treatment of Bilateral Refractive Amblyopia in Children Three to Less Than 10 Years of Age
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1. Heterozygous variants c.781G>A and c.1066dup of serine protease 56 cause familial nanophthalmos by impairing serine-type endopeptidase activity;British Journal of Ophthalmology;2022-04-05
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