Published in
Springer Nature [academic journals on nature.com], European Journal of Human Genetics, 12(24), p. 1730-1738, 2016
DOI: 10.1038/ejhg.2016.99
Links
Tools
An innovative strategy for the molecular diagnosis of Usher syndrome identifies causal biallelic mutations in 93% of European patients
Journal article published in 2016 by
Crystel Bonnet,
Zied Riahi,
Sandra Chantot-Bastaraud,
Luce Smagghe,
Mélanie Letexier,
Charles Marcaillou,
Gaëlle M. Lefèvre,
Jean-Pierre Hardelin,
Aziz El-Amraoui 
,
Amrit Singh-Estivalet,
Saddek Mohand-Saïd,
Susanne Kohl,
Anne Kurtenbach,
Ieva Sliesoraityte,
Ditta Zobor
and other authors.
,
Amrit Singh-Estivalet,
Saddek Mohand-Saïd,
Susanne Kohl,
Anne Kurtenbach,
Ieva Sliesoraityte,
Ditta Zobor
and other authors.
This paper is made freely available by the publisher.
Full text: Download
Published version:
archiving forbidden
Data provided by 