RAX and anophthalmia in humans: Evidence of brain anomalies

2012
Article

Résumé

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.

Source officielle

https://infoscience.epfl.ch/record/178751?ln=fr

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RAX and anophthalmia in humans: Evidence of brain anomalies

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