Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study

Wente, Sarah; Schroeder, Simone; Buckard, Johannes; Buettel, Hans-Martin; von Deimling, Florian; Diener, Wilfried; Haeussler, Martin; Huebschle, Susanne; Kinder, Silvia; Kurlemann, Gerhard; Kretzschmar, Christoph; Lingen, Michael; Maroske, Wiebke; Mundt, Dirk; Sanchez-Albisua, Iciar; Seeger, Juergen; Toelle, Sandra P.; Boltshauser, Eugen; Brockmann, Knut

Nosological delineation of congenital ocular motor apraxia type Cogan: an observational study

Autor(en):

Wente, Sarah; Schroeder, Simone; Buckard, Johannes; Buettel, Hans-Martin; von Deimling, Florian; Diener, Wilfried; Haeussler, Martin; Huebschle, Susanne; Kinder, Silvia; Kurlemann, Gerhard; Kretzschmar, Christoph; Lingen, Michael; Maroske, Wiebke; Mundt, Dirk; Sanchez-Albisua, Iciar; Seeger, Juergen; Toelle, Sandra P.; Boltshauser, Eugen; Brockmann, Knut

Tübinger Autor(en):

Sánchez-Albisua, Iciar

Erschienen in:

Orphanet Journal of Rare Diseases (2016), Bd. 11, Article 104

Verlagsangabe:

Biomed Central Ltd

Sprache:

Englisch

Referenz zum Volltext:

http://dx.doi.org/10.1186/s13023-016-0486-z

ISSN:

1750-1172