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Novel mutations in the KCNQ2 gene link epilepsy to a dysfunction of the KCNQ2-calmodulin interaction.
Richards, M C; Heron, S E; Spendlove, H E; Scheffer, I E; Grinton, B; Berkovic, S F; Mulley, J C; Davy, A.
Affiliation
  • Richards MC; Department of Laboratory Genetics, Women's and Children's Hospital, North Adelaide, South Australia, Australia.
J Med Genet ; 41(3): e35, 2004 Mar.
Article in En | MEDLINE | ID: mdl-14985406
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calmodulin / Potassium Channels / Epilepsy / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male / Newborn Language: En Journal: J Med Genet Year: 2004 Document type: Article Affiliation country: Australia
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Calmodulin / Potassium Channels / Epilepsy / Mutation Type of study: Prognostic_studies Limits: Female / Humans / Male / Newborn Language: En Journal: J Med Genet Year: 2004 Document type: Article Affiliation country: Australia