A novel mutation in KCNQ2-associated with BFNC, drug resistant epilepsy, and mental retardation

Neurology

Volumn 63, Issue 1, 2004, Pages 57-65

  Borgatti, Renato ^a   Zucca, C ^a   Cavallini, A ^a   Ferrario, M ^a   Panzeri, C ^a   Castaldo, P ^b   Soldovieri, M V ^b   Baschirotto, C ^a   Bresolin, N ^a,c   Bernardina, B Dalla ^d   Taglialatela, M ^b   Bassi, M T ^a  

^a SCIENTIFIC INSTITUTE   (Italy)

^b UNIVERSITY OF NAPLES FEDERICO II   (Italy)

^c UNIVERSITY OF MILAN   (Italy)

^d POLICLINICO BORGO ROMA   (Italy)

Author keywords

[No Author keywords available]

Indexed keywords

POTASSIUM CHANNEL;

ADULT; ARTICLE; AUTOSOMAL DOMINANT DISORDER; BENIGN CHILDHOOD EPILEPSY; BRAIN DISEASE; CARBOXY TERMINAL SEQUENCE; CELL MEMBRANE; CHILD; CHO CELL; CLINICAL ARTICLE; FEMALE; FOCAL EPILEPSY; GENE; GENE KCNQ2; GENE KCNQ3; GENE MUTATION; HEREDITY; HUMAN; MALE; MENTAL DEFICIENCY; MISSENSE MUTATION; NUCLEOTIDE SEQUENCE; PATHOPHYSIOLOGY; PHENOTYPIC VARIATION; POTASSIUM CURRENT; PRIORITY JOURNAL; PROTEIN BINDING;

EID: 3242701298     PISSN: 00283878     EISSN: None     Source Type: Journal    
DOI: 10.1212/01.WNL.0000132979.08394.6D     Document Type: Article

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