Literature DB >> 10908915

Glutamate decarboxylase is not genetically linked to pyridoxine-dependent seizures.

G Battaglioli1, D R Rosen, S M Gospe, D L Martin.   

Abstract

Several aspects of pyridoxine-dependent seizure (PDS) suggest a mutation affecting glutamate decarboxylase (GAD) as a possible cause. To examine the possibility of GAD linkage with PDS, the authors performed genotype analyses of three families using polymorphic markers near the GAD genes (GAD1 and GAD2). In each family, the affected siblings exhibited different genotypes for the GAD2 gene; in two families the GAD1 genotype was disparate. These findings suggest that a mutation of GAD is not directly involved in all cases of PDS.

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Year:  2000        PMID: 10908915     DOI: 10.1212/wnl.55.2.309

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


  9 in total

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Review 5.  New treatment paradigms in neonatal metabolic epilepsies.

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7.  Genetic heterogeneity for autosomal recessive pyridoxine-dependent seizures.

Authors:  C L Bennett; H M Huynh; P F Chance; I A Glass; S M Gospe
Journal:  Neurogenetics       Date:  2005-08-02       Impact factor: 2.660

Review 8.  Metabolic etiologies in West syndrome.

Authors:  Seda Salar; Solomon L Moshé; Aristea S Galanopoulou
Journal:  Epilepsia Open       Date:  2018-03-14

9.  Vitamin-responsive epileptic encephalopathies in children.

Authors:  Satish Agadi; Michael M Quach; Zulfi Haneef
Journal:  Epilepsy Res Treat       Date:  2013-07-25
  9 in total

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