Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness
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Title
Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness
Authors
Keywords
Cornea, X-linked traits, Nonsense mutation, X chromosomes, Deletion mutation, Genome-wide association studies, Glaucoma, Missense mutation
Journal
PLoS One
Volume 9, Issue 8, Pages e104163
Publisher
Public Library of Science (PLoS)
Online
2014-08-06
DOI
10.1371/journal.pone.0104163
References
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