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research article
RAX and anophthalmia in humans: Evidence of brain anomalies
2012
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.
Type
research article
Web of Science ID
WOS:000304981700002
Authors
Abouzeid, Hana
•
Youssef, Mohamed A.
•
Bayoumi, Nader
•
ElShakankiri, Nihal
•
Marzouk, Iman
•
Hauser, Philippe
•
Schorderet, Daniel F.
Publication date
2012
Published in
Volume
18
Start page
1449
End page
1456
Peer reviewed
REVIEWED
EPFL units
Available on Infoscience
June 29, 2012
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