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.


Published in:
Molecular Vision, 18, 1449-1456
Year:
2012
Keywords:
Laboratories:




 Record created 2012-06-29, last modified 2018-09-13


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