A reduced K+ current due to a novel mutation in KCNQ2 causes neonatal convulsions

Author:

Lerche H.,Biervert C.,Alekov A. K.,Schleithoff L.,Lindner M.,Klingler W.,Bretschneider F.,Mitrovic N.,Jurkat-Rott K.,Bode H.,Lehmann-Horn F.,Steinlein O. K.

Publisher

Wiley

Subject

Clinical Neurology,Neurology

Reference35 articles.

1. Seizure characteristics in chromosome 20 benign familial neonatal convulsions

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3. Benign idiopathic neonatal convulsions (familial and non-familial): open questions about these syndromes. In: ed. Epileptic seizures and syndromes. London: John Libbey, 1994: 193-201

4. Benign familial neonatal convulsions linked to genetic markers on chromosome 20

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