RAX and anophthalmia in humans: Evidence of brain anomalies

PURPOSE: To report the clinical and genetic study of two families of Egyptian origin with clinical anophthalmia. To further determine the role of the retina and anterior neural fold homeobox gene (RAX) in anophthalmia and associated cerebral malformations. METHODS: Three patients with clinical anoph...

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Detalles Bibliográficos
Autores principales: Abouzeid, Hana, Youssef, Mohamed A., Bayoumi, Nader, ElShakankiri, Nihal, Marzouk, Iman, Hauser, Philippe, Schorderet, Daniel F.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2012
Materias:
Research Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380941/
https://www.ncbi.nlm.nih.gov/pubmed/22736936

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3380941/
https://www.ncbi.nlm.nih.gov/pubmed/22736936

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