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 View Full Article

Authors

Keywords

Journal

EPILEPSIA

Volume 52, Issue 5, Pages 984-992

Publisher

Wiley

Online

2011-03-23

DOI

10.1111/j.1528-1167.2011.02980.x

References

View 1 related references

Ask authors/readers for more resources

Create your own webinar

Interested in hosting your own webinar? Check the schedule and propose your idea to the Peeref Content Team.

Create Now

Ask a Question. Answer a Question.

Quickly pose questions to the entire community. Debate answers and get clarity on the most important issues facing researchers.

Get Started

EPILEPSIA

Ask authors/readers for more resources

Protocol

Reagent

Reprint

Create your own webinar

Ask a Question. Answer a Question.