Literature DB >> 12874418

Polyalanine expansion of ARX associated with cryptogenic West syndrome.

M Kato1, S Das, K Petras, Y Sawaishi, W B Dobyns.   

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Year:  2003        PMID: 12874418     DOI: 10.1212/01.wnl.0000068012.69928.92

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


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  29 in total

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

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Review 7.  Pathogenesis and new candidate treatments for infantile spasms and early life epileptic encephalopathies: A view from preclinical studies.

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8.  CDKL5 and ARX mutations in males with early-onset epilepsy.

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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

Review 10.  Pathophysiology of epileptic encephalopathies.

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