LRP5 BIALLELIC MUTATIONS CAUSE A HIGHER INCIDENCE OF SEVERE PHENOTYPE COMPARED WITH LRP5 MONOALLELIC MUTATION
Author:
Publisher
Ovid Technologies (Wolters Kluwer Health)
Subject
Ophthalmology,General Medicine
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1. Clinical characteristics and mutation spectrum in 33 Chinese families with familial exudative vitreoretinopathy;Annals of Medicine;2022-11-21
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