Familial Whole Exome Sequencing Study of 30 Families With Early-Onset High Myopia
Investigative Ophthalmology & Visual Science2023Vol. 64(5), pp. 10–10
Citations Over TimeTop 10% of 2023 papers
Abstract
Candidate genes carried by patients with eoHM are closely related to inherited retinal diseases. Genetic screening in children with eoHM facilitates the early identification and intervention of syndromic hereditary ocular disorders and certain hereditary ophthalmopathies.
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