De Novo Mutations in GNAO1, Encoding a Gαo Subunit of Heterotrimeric G Proteins, Cause Epileptic Encephalopathy

American Journal of Human Genetics - United States
doi 10.1016/j.ajhg.2013.07.014
Full Text
Abstract

Available in full text

Categories
Genetics
Date
Authors
Publisher

Elsevier BV

Related search

A Lotus Japonicus cDNA Encoding an [Alpha] Subunit of a Heterotrimeric G-Protein

Plant Physiology
Plant ScienceGeneticsPhysiology
1994English

De Novo Pathogenic Variants in CACNA1E Cause Developmental and Epileptic Encephalopathy With Contractures, Macrocephaly, and Dyskinesias

American Journal of Human Genetics
Genetics
2019English

Domain-Opening and Dynamic Coupling in the Α-Subunit of Heterotrimeric G Proteins

Biophysical Journal
Biophysics
2013English

Loss-Of-Function Mutations in UDP-Glucose 6-Dehydrogenase Cause Recessive Developmental Epileptic Encephalopathy

Nature Communications
AstronomyGeneticsMolecular BiologyBiochemistryChemistryPhysics
2020English

Heterotrimeric G-Proteins: A Short History

British Journal of Pharmacology
Pharmacology
2009English

Heterotrimeric G Proteins in C. Elegans

WormBook
2006English

Gαo (GNAO1) Encephalopathies: Plasma Membrane vs. Golgi Functions

Oncotarget
Oncology
2017English

Accessory Proteins for Heterotrimeric G-Proteins in the Kidney

Frontiers in Physiology
Physiology
2015English

De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen Α2 Chain Cause Porencephaly

American Journal of Human Genetics
Genetics
2012English

Amanote Research

Note-taking for researchers

Follow Amanote

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

Privacy PolicyRefund Policy