Literature DB >> 12874405

ARX mutations in X-linked lissencephaly with abnormal genitalia.

G Uyanik1, L Aigner, P Martin, C Gross, D Neumann, H Marschner-Schäfer, U Hehr, J Winkler.   

Abstract

X-linked lissencephaly with abnormal genitalia (XLAG) is a distinct form of lissencephaly associated with absent corpus callosum. Recently, forms of syndromic and nonspecific X-linked mental retardation have been found to be associated with mutations in the Aristaless-related homeobox gene ARX. The authors assessed ARX as a candidate gene for XLAG in a genetic analysis of neuronal migration disorders and found two different point mutations in two XLAG pedigrees affecting the homeodomain of the protein, confirming that ARX is a causative gene for XLAG.

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Year:  2003        PMID: 12874405     DOI: 10.1212/01.wnl.0000079371.19562.ba

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  20 in total

1.  Familial West syndrome and dystonia caused by an Aristaless related homeobox gene mutation.

Authors:  Gabriele Wohlrab; Goekhan Uyanik; Claudia Gross; Ute Hehr; Jürgen Winkler; Bernhard Schmitt; Eugen Boltshauser
Journal:  Eur J Pediatr       Date:  2005-02-22       Impact factor: 3.183

2.  Screening of ARX in mental retardation families: Consequences for the strategy of molecular diagnosis.

Authors:  K Poirier; D Lacombe; B Gilbert-Dussardier; M Raynaud; V Desportes; A P M de Brouwer; C Moraine; J P Fryns; H H Ropers; C Beldjord; J Chelly; T Bienvenu
Journal:  Neurogenetics       Date:  2005-10-19       Impact factor: 2.660

3.  Clinical Images: Postterm Newborn with Lissencephaly Presented with Seizure: Case Report and Review of Literature.

Authors:  Mustafa Alhasan; Mansour Mathkour; James M Milburn
Journal:  Ochsner J       Date:  2015

4.  Fetal and neonatal MRI features of ARX-related lissencephaly presenting with neonatal refractory seizure disorder.

Authors:  Sara Ffrench-Constant; Carolina Kachramanoglou; Brynmor Jones; Nigel Basheer; Nikolaos Syrmos; Mario Ganau; Wajanat Jan
Journal:  Quant Imaging Med Surg       Date:  2019-11

Review 5.  Genetics, molecular biology, and phenotypes of x-linked epilepsy.

Authors:  Hao Deng; Wen Zheng; Zhi Song
Journal:  Mol Neurobiol       Date:  2013-11-22       Impact factor: 5.590

6.  Novel NDE1 homozygous mutation resulting in microhydranencephaly and not microlyssencephaly.

Authors:  Ayse Guven; Aysegul Gunduz; Tarik M Bozoglu; Cengiz Yalcinkaya; Aslıhan Tolun
Journal:  Neurogenetics       Date:  2012-04-15       Impact factor: 2.660

Review 7.  Fragile X and X-linked intellectual disability: four decades of discovery.

Authors:  Herbert A Lubs; Roger E Stevenson; Charles E Schwartz
Journal:  Am J Hum Genet       Date:  2012-04-06       Impact factor: 11.025

8.  Mutations in the nuclear localization sequence of the Aristaless related homeobox; sequestration of mutant ARX with IPO13 disrupts normal subcellular distribution of the transcription factor and retards cell division.

Authors:  Cheryl Shoubridge; May Huey Tan; Tod Fullston; Desiree Cloosterman; David Coman; George McGillivray; Grazia M Mancini; Tjitske Kleefstra; Jozef Gécz
Journal:  Pathogenetics       Date:  2010-01-05

9.  Mutations in ARX Result in Several Defects Involving GABAergic Neurons.

Authors:  Gaëlle Friocourt; John G Parnavelas
Journal:  Front Cell Neurosci       Date:  2010-03-11       Impact factor: 5.505

10.  Reinitiation of mRNA translation in a patient with X-linked infantile spasms with a protein-truncating variant in ARX.

Authors:  Ching Moey; Scott Topper; Mary Karn; Amy Knight Johnson; Soma Das; Jorge Vidaurre; Cheryl Shoubridge
Journal:  Eur J Hum Genet       Date:  2015-08-26       Impact factor: 4.246

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