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

BACKGROUND: The nosological assignment of congenital ocular motor apraxia type Cogan (COMA) is still controversial. While regarded as a distinct entity by some authorities including the Online Mendelian Inheritance in Man catalog of genetic disorders, others consider COMA merely a clinical symptom....

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Detalles Bibliográficos
Autores principales: Wente, Sarah, Schröder, Simone, Buckard, Johannes, Büttel, Hans-Martin, von Deimling, Florian, Diener, Wilfried, Häussler, Martin, Hübschle, Susanne, Kinder, Silvia, Kurlemann, Gerhard, Kretzschmar, Christoph, Lingen, Michael, Maroske, Wiebke, Mundt, Dirk, Sánchez-Albisua, Iciar, Seeger, Jürgen, Toelle, Sandra P., Boltshauser, Eugen, Brockmann, Knut
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Research
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966602/
https://www.ncbi.nlm.nih.gov/pubmed/27473762
http://dx.doi.org/10.1186/s13023-016-0486-z

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4966602/
https://www.ncbi.nlm.nih.gov/pubmed/27473762
http://dx.doi.org/10.1186/s13023-016-0486-z

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