Mutations in IMPG1 Cause Vitelliform Macular Dystrophies

Manes, Gael; Meunier, Isabelle; Avila-Fernandez, Almudena; Banfi, Sandro; Le Meur, Guylene; Zanlonghi, Xavier; Corton, Marta; Simonelli, Francesca; Brabet, Philippe; Labesse, Gilles; Audo, Isabelle; Mohand-Said, Saddek; Zeitz, Christina; Sahel, Jose-Alain; Weber, Michel; Dollfus, Helene; Dhaenens, Claire-Marie; Allorge, Delphine; De Baere, Elfride; Koenekoop, Robert K.; Kohl, Susanne; Cremers, Frans P. M.; Hollyfield, Joe G.; Senechal, Audrey; Hebrard, Maxime; Bocquet, Beatrice; Ayuso Garcia, Carmen; Hamel, Christian P.

Mutations in IMPG1 Cause Vitelliform Macular Dystrophies

Autor(en):

Manes, Gael; Meunier, Isabelle; Avila-Fernandez, Almudena; Banfi, Sandro; Le Meur, Guylene; Zanlonghi, Xavier; Corton, Marta; Simonelli, Francesca; Brabet, Philippe; Labesse, Gilles; Audo, Isabelle; Mohand-Said, Saddek; Zeitz, Christina; Sahel, Jose-Alain; Weber, Michel; Dollfus, Helene; Dhaenens, Claire-Marie; Allorge, Delphine; De Baere, Elfride; Koenekoop, Robert K.; Kohl, Susanne; Cremers, Frans P. M.; Hollyfield, Joe G.; Senechal, Audrey; Hebrard, Maxime; Bocquet, Beatrice; Ayuso Garcia, Carmen; Hamel, Christian P.

Tübinger Autor(en):

Kohl, Susanne

Erschienen in:

American Journal of Human Genetics (2013), Bd. 93, H. 3, S. 571-578

Verlagsangabe:

Cell Press

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1016/j.ajhg.2013.07.018

ISSN:

0002-9297