Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Zeitz, Christina; Jacobson, Samuel G.; Hamel, Christian P.; Bujakowska, Kinga; Neuille, Marion; Orhan, Elise; Zanlonghi, Xavier; Lancelot, Marie-Elise; Michiels, Christelle; Schwartz, Sharon B.; Bocquet, Beatrice; Antonio, Aline; Audier, Claire; Letexier, Melanie; Saraiva, Jean-Paul; Luu, Tien D.; Sennlaub, Florian; Nguyen, Hoan; Poch, Olivier; Dollfus, Helene; Lecompte, Odile; Kohl, Susanne; Sahel, Jose-Alain; Bhattacharya, Shomi S.; Audo, Isabelle

Whole-Exome Sequencing Identifies LRIT3 Mutations as a Cause of Autosomal-Recessive Complete Congenital Stationary Night Blindness

Autor(en):

Zeitz, Christina; Jacobson, Samuel G.; Hamel, Christian P.; Bujakowska, Kinga; Neuille, Marion; Orhan, Elise; Zanlonghi, Xavier; Lancelot, Marie-Elise; Michiels, Christelle; Schwartz, Sharon B.; Bocquet, Beatrice; Antonio, Aline; Audier, Claire; Letexier, Melanie; Saraiva, Jean-Paul; Luu, Tien D.; Sennlaub, Florian; Nguyen, Hoan; Poch, Olivier; Dollfus, Helene; Lecompte, Odile; Kohl, Susanne; Sahel, Jose-Alain; Bhattacharya, Shomi S.; Audo, Isabelle

Tübinger Autor(en):

Kohl, Susanne

Erschienen in:

American Journal of Human Genetics (2013), Bd. 92, H. 1, S. 67-75

Verlagsangabe:

Cell Press

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1016/j.ajhg.2012.10.023

ISSN:

0002-9297