Literature DB >> 15707237

The phenotypic spectrum of ARX mutations.

Mohnish Suri1.   

Abstract

Mutations in the ARX gene can result in many different phenotypes, including phenotypes associated with severe brain malformations and less severe phenotypes associated with syndromic or non-syndromic forms of XLMR. There seems to be a consistent genotype-phenotype correlation and both interfamilial and intrafamilial variability of expression of some of the mutations, particularly the common 428-451dup(24 bp) mutation. Familiarity with the phenotypic spectrum of ARX mutations is helpful in determining when to request ARX mutation analysis.

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Year:  2005        PMID: 15707237     DOI: 10.1017/s001216220500023x

Source DB:  PubMed          Journal:  Dev Med Child Neurol        ISSN: 0012-1622            Impact factor:   5.449


  8 in total

1.  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

Review 2.  Clinical, genetic and imaging findings identify new causes for corpus callosum development syndromes.

Authors:  Timothy J Edwards; Elliott H Sherr; A James Barkovich; Linda J Richards
Journal:  Brain       Date:  2014-01-28       Impact factor: 13.501

3.  Mutation screening of the ARX gene in patients with autism.

Authors:  Pauline Chaste; Gudrun Nygren; Henrik Anckarsäter; Maria Råstam; Mary Coleman; Marion Leboyer; Christopher Gillberg; Catalina Betancur
Journal:  Am J Med Genet B Neuropsychiatr Genet       Date:  2007-03-05       Impact factor: 3.568

4.  Conditional Loss of Arx From the Developing Dorsal Telencephalon Results in Behavioral Phenotypes Resembling Mild Human ARX Mutations.

Authors:  Jacqueline C Simonet; C Nicole Sunnen; Jue Wu; Jeffrey A Golden; Eric D Marsh
Journal:  Cereb Cortex       Date:  2014-05-02       Impact factor: 5.357

5.  The axis of progression of disease.

Authors:  Alan M Tartakoff; Di Wu
Journal:  Cancer Inform       Date:  2014-10-19

6.  Screening of the duplication 24 pb of ARX gene in Moroccan patients with X-linked Intellectual Disability.

Authors:  Yousra Benmakhlouf; Renaud Touraine; Ines Harzallah; Zeineb Zian; Kaoutar Ben Makhlouf; Amina Barakat; Naima Ghailani Nourouti; Mohcine Bennani Mechita
Journal:  BMC Res Notes       Date:  2021-03-23

7.  Development and validation of a multiplex-PCR assay for X-linked intellectual disability.

Authors:  Paula Jorge; Bárbara Oliveira; Isabel Marques; Rosário Santos
Journal:  BMC Med Genet       Date:  2013-08-05       Impact factor: 2.103

Review 8.  Chromatin Remodeling Proteins in Epilepsy: Lessons From CHD2-Associated Epilepsy.

Authors:  Kay-Marie J Lamar; Gemma L Carvill
Journal:  Front Mol Neurosci       Date:  2018-06-15       Impact factor: 5.639

  8 in total

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