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Fmr1 and autism, an intriguing connection revisited
William Fyke, Milen Velinov
Research output
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Contribution to journal
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Review article
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peer-review
22
Scopus citations
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Keyphrases
Autism Spectrum Disorder
100%
Autism
100%
Fragile X Mental Retardation 1 (FMR1)
100%
Fragile X Syndrome
88%
Genetic Heterogeneity
11%
Central Nervous System
11%
Multiple Pathways
11%
US Population
11%
Loss Function
11%
Major Gene
11%
5′-untranslated Region (5′-UTR)
11%
Severe Manifestations
11%
Single Gene Disorders
11%
Protein Drug
11%
CGG Repeat
11%
Stereotypic Behavior
11%
Chromosome X
11%
Behavioral Dysfunction
11%
Communication Behavior
11%
Gene Regulators
11%
Biochemistry, Genetics and Molecular Biology
FMR1
100%
Genetic Heterogeneity
33%
X Chromosome
33%
Untranslated Region
33%
Major Gene
33%
Regulatory Gene
33%
Single Gene Disorder
33%
Neuroscience
Pervasive Developmental Disorder
100%
Fragile X Syndrome
88%
Behavior (Neuroscience)
11%
Central Nervous System
11%
Major Gene
11%
X Chromosome
11%
Untranslated Region
11%