Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions. | Neurosci Lett;462(1): 24-9, 2009 Oct 02. | MEDLINE

Main content 1 Search 2 Footer 3

+A A -A High contrast

VHL Regional Portal

Information and Knowledge for Health

Advanced Search EVID@Easy

Functional analysis of novel KCNQ2 mutations found in patients with Benign Familial Neonatal Convulsions.

Volkers, Linda; Rook, Martin B; Das, Joost H G; Verbeek, Nienke E; Groenewegen, W Antoinette; van Kempen, Marjan J A; Lindhout, Dick; Koeleman, Bobby P C.

Affiliation

Volkers L; Complex Genetics Section, DBG-Department of Medical Genetics, University Medical Center Utrecht, The Netherlands.

Neurosci Lett ; 462(1): 24-9, 2009 Oct 02.

Article in En | MEDLINE | ID: mdl-19559753

Subject(s)

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Benign Neonatal / KCNQ2 Potassium Channel Limits: Female / Humans Language: En Journal: Neurosci Lett Year: 2009 Document type: Article Affiliation country: Países Bajos Country of publication: Irlanda

Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Epilepsy, Benign Neonatal / KCNQ2 Potassium Channel Limits: Female / Humans Language: En Journal: Neurosci Lett Year: 2009 Document type: Article Affiliation country: Países Bajos Country of publication: Irlanda