A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females-Reference-Cited by-同舟云学术

A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and neuropsychiatric disorders in females

Published:2011-03-22 Issue:5 Volume:52 Page:984-992
ISSN:0013-9580
Container-title:Epilepsia
language:en
Short-container-title:

Author:

Ekşioğlu Yaman Z.,Pong Amanda W.,Takeoka Masanori

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1528-1167.2011.02980.x/fullpdf

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4. The simultaneous loss of Arx and Pax4 genes promotes a somatostatin-producing cell fate specification at the expense of the alpha- and beta-cell lineages in the mouse endocrine pancreas;Collombat;Development,2005

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