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

YZ Ekşioğlu, AW Pong, M Takeoka - Epilepsia, 2011 - Wiley Online Library
Purpose: ARX, the aristaless‐related homeobox gene, is implicated in cerebral, testicular,
and pancreatic development. ARX mutations are associated with various forms of epilepsy …

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

YZ Ekşioğlu, AW Pong, M Takeoka - Epilepsia, 2011 - europepmc.org
Purpose ARX, the aristaless-related homeobox gene, is implicated in cerebral, testicular,
and pancreatic development. ARX mutations are associated with various forms of epilepsy …

[引用][C] A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and …

YZ EKSIOGLU, AW PONG… - Epilepsia …, 2011 - pascal-francis.inist.fr
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 …

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

YZ Ekşioğlu, AW Pong, M Takeoka - Epilepsia, 2011 - infona.pl
Purpose: ARX, the aristaless‐related homeobox gene, is implicated in cerebral, testicular,
and pancreatic development. ARX mutations are associated with various forms of epilepsy …

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

YZ Ekşioğlu, AW Pong, M Takeoka - Epilepsia, 2011 - pubmed.ncbi.nlm.nih.gov
Purpose ARX, the aristaless-related homeobox gene, is implicated in cerebral, testicular,
and pancreatic development. ARX mutations are associated with various forms of epilepsy …

[引用][C] A novel mutation in the aristaless domain of the ARX gene leads to Ohtahara syndrome, global developmental delay, and ambiguous genitalia in males and …

YZ EKSIOGLU, AW PONG, M TAKEOKA - Epilepsia, 2011 - Wiley-Blackwell