DOI:
10.1055/s-00029030
Journal of Pediatric Neurology
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References
Ekşioğlu YZ, Pong AW, Takeoka M.
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.
Epilepsia 2011;
52 (05) 984-992
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