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
Author(s)
Abouzeid, Hana
Youssef, Mohamed A.
Bayoumi, Nader
ElShakankiri, Nihal
Marzouk, Iman
Hauser, Philippe
Schorderet, Daniel F.
Date Issued
2012
Published in
Volume
18
Start page
1449
End page
1456
Editorial or Peer reviewed
REVIEWED
Written at
EPFL
EPFL units
Available on Infoscience
June 29, 2012
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