Publication
Title
Broadening the phenotype of LRP2 mutations: a new mutation in LRP2 causes a predominantly ocular phenotype suggestive of Stickler syndrome
Author
Abstract
Language
English
Source (journal)
Clinical genetics. - Copenhagen
Publication
Copenhagen : 2014
ISSN
0009-9163
Volume/pages
86:3(2014), p. 282-286
ISI
000340892300014
Full text (Publisher's DOI)
Full text (publisher's version - intranet only)
UAntwerpen
Faculty/Department
Research group
Project info
Belgian medical genomics initiative (BeMGI).
Publication type
Subject
Affiliation
Publications with a UAntwerp address
External links
Web of Science
Record
Identification
Creation 09.10.2014
Last edited 21.11.2018
To cite this reference