SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1

Literature (3)

Literature for OMIM 121200: SEIZURES, BENIGN FAMILIAL NEONATAL, 1; BFNS1

Xenbase Articles:
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Neutralization of a negative charge in the S1-S2 region of the KV7.2 (KCNQ2) channel affects voltage-dependent activation in neonatal epilepsy., Wuttke TV,Penzien J,Fauler M,Seebohm G,Lehmann-Horn F,Lerche H,Jurkat-Rott K, J Physiol. January 15, 2008; 586(2):0022-3751.
Channelopathies: ion channel defects linked to heritable clinical disorders., Felix R, J Med Genet. October 1, 2000; 37(10):1468-6244.
Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures., Maljevic S,Vejzovic S,Bernhard MK,Bertsche A,Döcker M,Lemke JR,Merkenschlager A,Weise S,Lerche H,Syrbe S, Mol Syndromol. September 1, 2016; 7(4):1661-8769.

Channelopathies: ion channel defects linked to heritable clinical disorders., Felix R, J Med Genet. October 1, 2000; 37(10):1468-6244.

Novel KCNQ3 Mutation in a Large Family with Benign Familial Neonatal Epilepsy: A Rare Cause of Neonatal Seizures., Maljevic S,Vejzovic S,Bernhard MK,Bertsche A,Döcker M,Lemke JR,Merkenschlager A,Weise S,Lerche H,Syrbe S, Mol Syndromol. September 1, 2016; 7(4):1661-8769.