Sort by
Keyphrases
Movement Disorders
100%
Missense mutation
100%
Infantile Epileptic Encephalopathy
100%
Choreiform Movement
100%
GABRA2
100%
De-novo mutations
40%
Autosomal Dominant
40%
GABAA Receptor (GABAAR)
40%
Vision Impairment
40%
Convulsive Disorders
40%
Family Planning
20%
Jewish Population
20%
Family History
20%
Gene number
20%
Ashkenazi Jews
20%
Implications for Treatment
20%
Neurological Diseases
20%
Genetic Diagnosis
20%
Whole Exome Sequencing
20%
Treatment Planning
20%
Biological Basis
20%
Epileptic Syndromes
20%
Genetic Causes
20%
Hypotonia
20%
Conserved Domain
20%
Male Infant
20%
Heterozygous Missense mutation
20%
Movement Impairment
20%
GABRA1
20%
GABRB1
20%
Neonatal Hypothermia
20%
GABRB3
20%
GABRG2
20%
Medicine and Dentistry
Epilepsy
100%
Brain Disease
100%
Missense Mutation
100%
Stereotypic Movement Disorder
100%
GABRA2
100%
Visual Impairment
33%
Convulsion
33%
Autosomal Dominant Inheritance
33%
GABAA Receptor
33%
Disease
16%
Family Planning
16%
Hypotonia
16%
Family History
16%
Neurologic Disease
16%
Treatment Planning
16%
Exome Sequencing
16%
GABRB1
16%
GABRG2
16%
GABRB3
16%
Hypothermia
16%
Neuroscience
Encephalopathy
100%
Missense Mutation
100%
GABRA2
100%
Stereotypic Movement Disorder
100%
GABAA Receptor
40%
Nervous System Disorder
20%
Hypothermia
20%
Hypotonia
20%
GABRG2
20%
GABRB1
20%
GABRB3
20%
Exome Sequencing
20%
Biochemistry, Genetics and Molecular Biology
Missense Mutation
100%
GABRA2
100%
Genetics
50%
Autosomal Dominant Inheritance
50%
GABAA Receptor
50%
Exome Sequencing
25%
GABRB1
25%
Hypothermia
25%
GABRB3
25%
GABRG2
25%