Recessive Mutations inLEPREL1Underlie a Recognizable Lens Subluxation Phenotype
Author:
Publisher
Informa UK Limited
Subject
Genetics(clinical),Ophthalmology,Pediatrics, Perinatology, and Child Health
Link
http://www.tandfonline.com/doi/pdf/10.3109/13816810.2014.985847
Reference24 articles.
1. Results of fibrillin-1 gene analysis in children from inbred families with lens subluxation
2. Autozygome decoded
3. High Myopia Caused by a Mutation in LEPREL1, Encoding Prolyl 3-Hydroxylase 2
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