An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. [electronic resource]
Producer: 20170621Description: 757-71 p. digitalISSN:- 1432-1203
- Adolescent
- Adult
- Aged
- Animals
- Autistic Disorder -- genetics
- Chromosome Deletion
- Chromosomes, Human, Pair 12 -- genetics
- Comparative Genomic Hybridization
- Disease Models, Animal
- Epilepsy -- genetics
- F-Box Proteins -- genetics
- Female
- Fetus
- Histone-Lysine N-Methyltransferase -- genetics
- Humans
- In Situ Hybridization, Fluorescence
- Intellectual Disability -- genetics
- Jumonji Domain-Containing Histone Demethylases -- genetics
- Male
- Middle Aged
- Zebrafish
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Publication Type: Journal Article
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