RAX and anophthalmia in humans: Evidence of brain anomalies
2012
Abstract
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.
Details
Title
RAX and anophthalmia in humans: Evidence of brain anomalies
Author(s)
Abouzeid, Hana ; Youssef, Mohamed A. ; Bayoumi, Nader ; ElShakankiri, Nihal ; Marzouk, Iman ; Hauser, Philippe ; Schorderet, Daniel F.
Published in
Molecular Vision
Volume
18
Pages
1449-1456
Date
2012
Keywords
Other identifier(s)
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Laboratories
SV
Record Appears in
Scientific production and competences > Unattributed publications > SV - SV - Unattributed publications
Scientific production and competences > SV - School of Life Sciences > SV - Unattributed publications
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Scientific production and competences > SV - School of Life Sciences > SV - Unattributed publications
Peer-reviewed publications
Work produced at EPFL
Journal Articles
Published
Record creation date
2012-06-29