Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness - Paulina

Login with Wikimedia

Login with your Wikimedia account to add/edit data Login

Missing/wrong data? Log in to edit

Image of a generic work. The text above it indicates that there is no free image of the work available, and that if you own one, you can click on the placeholder link to upload it.

Association of CHRDL1 mutations and variants with X-linked megalocornea, Neuhäuser syndrome and central corneal thickness

scientific article published in 2014

Author/s

author: Vincent Plagnol, Sek-Shir Cheong, Cristina Venturini, Nicole Carnt, Tom R Webb, Jens M Hertz, Christopher J. Hammond, Alison Hardcastle, Marie Restori, Daniela T Pilz

Work details

Publication date

2014

Language

English

Copyright status

copyrighted