Autosomal Dominant Form Of Benign Neonatal Seizures

Overview of Autosomal Dominant Form Of Benign Neonatal Seizures

Most recent studies have shown that Autosomal Dominant Form Of Benign Neonatal Seizures shares some biological mechanisms with absence-epilepsy, benign-neonatal-epilepsy, channelopathies, convulsion-neonatal, convulsions, epilepsies-myoclonic, epilepsies-partial, epilepsy, epilepsy-frontal-lobe, epilepsy-generalized, epilepsy-temporal-lobe, familial-benign-neonatal-epilepsy, febrile-convulsions, infantile-spasms, isaacs-syndrome, long-qt-syndrome, nervousness, pain.

Among the many pathways, these few ones have gauged particular interests from scientists studying Autosomal Dominant Form Of Benign Neonatal Seizures, and have been seen in publications frequently: Localization, Pathogenesis

Quite a number of genes have been found to play important roles in Autosomal Dominant Form Of Benign Neonatal Seizures, such as CA1, CD1A, CHRNA4, CLCN2, GJB3, KCNC4, KCNE2, KCNJ1, KCNJ2, KCNQ1, KCNQ2, KCNQ3, KCNQ4, KCNQ5, PEPD, SCN1A, SCN1B, SCN2A, SCN5A, SCN9A. See what Boster has to offer for the research of these genes by clicking the gene name links below and view a more detailed info card/product listing for that gene.

In a later update, we will include information such as current drugs and therapy solutions as well as on-going and past clinical trials for this disease. Plesae stay updated.

Autosomal Dominant Form Of Benign Neonatal Seizures Related Genes

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Pathways Related to Autosomal Dominant Form Of Benign Neonatal Seizures

This information is being compiled and will come in a future update

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