Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness-Reference-Cited by-同舟云学术

Association of CHRDL1 Mutations and Variants with X-linked Megalocornea, Neuhäuser Syndrome and Central Corneal Thickness

Published:2014-08-05 Issue:8 Volume:9 Page:e104163
ISSN:1932-6203
Container-title:PLoS ONE
language:en
Short-container-title:PLoS ONE

Author:

Davidson Alice E.,Cheong Sek-Shir,Hysi Pirro G.,Venturini Cristina,Plagnol Vincent,Ruddle Jonathan B.,Ali Hala,Carnt Nicole,Gardner Jessica C.,Hassan Hala,Gade Else,Kearns Lisa,Jelsig Anne Marie,Restori Marie,Webb Tom R.,Laws David,Cosgrove Michael,Hertz Jens M.,Russell-Eggitt Isabelle,Pilz Daniela T.,Hammond Christopher J.,Tuft Stephen J.,Hardcastle Alison J.

Publisher

Public Library of Science (PLoS)

Subject

Multidisciplinary

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