Genetic modifiers of neurological disease
Author:
Publisher
Elsevier BV
Subject
Developmental Biology,Genetics
Reference54 articles.
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1. Fine mapping and candidate gene analysis of Dravet syndrome modifier loci on mouse chromosomes 7 and 8;Mammalian Genome;2024-06-11
2. SCN1A Channels a Wide Range of Epileptic Phenotypes: Report of Novel and Known Variants with Variable Presentations;International Journal of Molecular Sciences;2024-05-22
3. Fine Mapping and Candidate Gene Analysis of Dravet Syndrome Modifier Loci on Mouse Chromosomes 7 and 8;2024-04-18
4. Mechanisms underlying the efficacy and limitation of dopa and tetrahydrobiopterin therapies for the deficiency of GTP cyclohydrolase 1 revealed in a novel mouse model;European Journal of Pharmacology;2024-03
5. Heterozygous deletion of Gpr55 does not affect a hyperthermia-induced seizure, spontaneous seizures or survival in the Scn1a+/- mouse model of Dravet syndrome;PLOS ONE;2023-01-26
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