L Dudler
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View article: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …
View article: Author response: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Author response: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …
View article: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …
View article: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …
View article: Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy
Plural molecular and cellular mechanisms of pore domain KCNQ2 encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …
View article: Plural molecular and cellular mechanisms of pore domain <i>KCNQ2</i> encephalopathy
Plural molecular and cellular mechanisms of pore domain <i>KCNQ2</i> encephalopathy Open
KCNQ2 variants in children with neurodevelopmental impairment are difficult to assess due to their heterogeneity and unclear pathogenic mechanisms. We describe a child with neonatal-onset epilepsy, developmental impairment of intermediate …