An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability.

Labonne, Jonathan D J

An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. [electronic resource] - Human genetics 07 2016 - 757-71 p. digital

Publication Type: Journal Article

1432-1203

10.1007/s00439-016-1668-4 doi


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