Keyphrases
CUX1
100%
Genotype-phenotype
100%
Underlying Pathology
100%
Neurodevelopmental Disorders
100%
Intellectual Disability
18%
Seizure
18%
Leading Symptoms
9%
Delayed Speech Development
9%
Nonsyndromic
9%
Phenotypic Data
9%
Increased Vulnerability
9%
Forehead
9%
Molecular Mechanism
9%
Developmental Stages
9%
Moderate Intellectual Disability
9%
Molecular Information
9%
Epilepsy
9%
Normal Brain
9%
Adulthood
9%
Muscular Hypotonia
9%
Moderate to Severe
9%
Clinical Presentation
9%
Cause of Disease
9%
Missense Variants
9%
Joint Laxity
9%
Post-transcriptional
9%
Mouse Model
9%
Syndromic Phenotypes
9%
Clinical Course
9%
Developmental Delay
9%
Delayed Psychomotor Development
9%
Early Postnatal
9%
Delayed Development
9%
International Collaboration
9%
Global Developmental Delay
9%
Biochemistry, Genetics and Molecular Biology
Intellectual Disability
100%
Genotyping
100%
Mouse
66%
Mouse Model
33%
Speech Development
33%
Motor Development
33%
Developmental Stage
33%
Missense
33%
