Dissecting the Genetic Basis of Comorbid Epilepsy Phenotypes in Neurodevelopmental Disorders

Genome Medicine - United Kingdom
doi 10.1186/s13073-019-0678-y
Full Text
Abstract

Available in full text

Date
Authors
Publisher

Springer Science and Business Media LLC

Related search

Mapping a Shared Genetic Basis for Neurodevelopmental Disorders

Genome Medicine
Molecular MedicineGeneticsMolecular Biology
2017English

Diagnostic Outcomes for Genetic Testing of 70 Genes in 8565 Patients With Epilepsy and Neurodevelopmental Disorders

Epilepsia
Neurology
2018English

Comorbid Mental Disorders in Anxiety Disorders: Genetic Aspects of Bipolar Disorders and of Ethnicity

2016English

Emerging Role of the Autophagy/Lysosomal Degradative Pathway in Neurodevelopmental Disorders With Epilepsy

Frontiers in Cellular Neuroscience
Molecular NeuroscienceCellular
2020English

Heterozygous Variants in KMT2E Cause a Spectrum of Neurodevelopmental Disorders and Epilepsy

American Journal of Human Genetics
Genetics
2019English

Genetic Basis of Sleep Disorders

Schweizer Archiv für Neurologie und Psychiatrie
2003English

Genetic and Neurodevelopmental Spectrum ofSYNGAP1-associated Intellectual Disability and Epilepsy

Journal of Medical Genetics
Genetics
2016English

Quantitative Genetic Basis of Arterial Phenotypes in the Brown Norway Rat

Physiological Genomics
GeneticsPhysiology
2007English

Genetic Basis of Dental Disorders: A Review

Journal of Oral Health and Community Dentistry
2008English

Amanote Research

Note-taking for researchers

Follow Amanote

© 2024 Amaplex Software S.P.R.L. All rights reserved.

Privacy PolicyRefund Policy