Copyright © 2004 by the BMJ Publishing Group Ltd.M C Richards, S E Heron, H E Spendlove, I E Scheffer, B Grinton, S F Berkovic, J C Mulley, A Dav
KCNQ5 is a highly conserved gene encoding an important channel for neuronal function; it is widely e...
Complex neurodevelopmental syndromes frequently have an unknown etiology, in which genetic factors p...
OBJECTIVE: To identify the genetic basis of a family segregating episodic ataxia, infantile seizures...
BACKGROUND: Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused ...
Background: Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused ...
Potassium channel subunits encoded by several genes of the KCNQ family underlie the M-current. Speci...
Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in...
dissertationBenign Familial Neonatal Convulsions (BFNC) is a human pediatric epilepsy characterized ...
Among neonatal epileptic syndromes, benign familial neonatal seizures (BFNS) are often due to autoso...
Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations...
KCNQ2 and KCNQ3 K+ channel subunits underlie the muscarinic-regulated K+ current (I(KM)), a widespre...
Objective: KCNQ2 and KCNQ3 mutations are known to be responsible for benign familial neonatal seizur...
Benign familial neonatal convulsions (BFNC) are characterized by unprovoked seizures during the firs...
Complex neurodevelopmental syndromes frequently have an unknown etiology, in which genetic factors p...
Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant generalized epilepsy of the...
KCNQ5 is a highly conserved gene encoding an important channel for neuronal function; it is widely e...
Complex neurodevelopmental syndromes frequently have an unknown etiology, in which genetic factors p...
OBJECTIVE: To identify the genetic basis of a family segregating episodic ataxia, infantile seizures...
BACKGROUND: Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused ...
Background: Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused ...
Potassium channel subunits encoded by several genes of the KCNQ family underlie the M-current. Speci...
Mutations in the KCNQ2 gene encoding for voltage-gated potassium channel subunits have been found in...
dissertationBenign Familial Neonatal Convulsions (BFNC) is a human pediatric epilepsy characterized ...
Among neonatal epileptic syndromes, benign familial neonatal seizures (BFNS) are often due to autoso...
Benign familial neonatal convulsion (BFNC) is a rare autosomal dominant disorder caused by mutations...
KCNQ2 and KCNQ3 K+ channel subunits underlie the muscarinic-regulated K+ current (I(KM)), a widespre...
Objective: KCNQ2 and KCNQ3 mutations are known to be responsible for benign familial neonatal seizur...
Benign familial neonatal convulsions (BFNC) are characterized by unprovoked seizures during the firs...
Complex neurodevelopmental syndromes frequently have an unknown etiology, in which genetic factors p...
Benign familial neonatal convulsions (BFNC) is a rare autosomal dominant generalized epilepsy of the...
KCNQ5 is a highly conserved gene encoding an important channel for neuronal function; it is widely e...
Complex neurodevelopmental syndromes frequently have an unknown etiology, in which genetic factors p...
OBJECTIVE: To identify the genetic basis of a family segregating episodic ataxia, infantile seizures...
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