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Glutamate decarboxylase is not genetically linked to pyridoxine-dependent seizures.
Battaglioli, G; Rosen, D R; Gospe, S M; Martin, D L.
Affiliation
  • Battaglioli G; Wadsworth Center, New York State Department of Health, Albany, USA. battagli@wadsworth.org
Neurology ; 55(2): 309-11, 2000 Jul 25.
Article in En | MEDLINE | ID: mdl-10908915
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.
Subject(s)
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Collection: 01-internacional Database: MEDLINE Main subject: Pyridoxine / Vitamin B 6 Deficiency / Spasms, Infantile / Genotype / Glutamate Decarboxylase / Genetic Linkage Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Neurology Year: 2000 Document type: Article
Search on Google
Collection: 01-internacional Database: MEDLINE Main subject: Pyridoxine / Vitamin B 6 Deficiency / Spasms, Infantile / Genotype / Glutamate Decarboxylase / Genetic Linkage Limits: Child / Child, preschool / Female / Humans / Infant / Male / Newborn Language: En Journal: Neurology Year: 2000 Document type: Article