Condition: INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
rs886037864
in
BCL11A
gene and
INTELLECTUAL DEVELOPMENTAL DISORDER WITH PERSISTENCE OF FETAL HEMOGLOBIN
PMID 27453576
2016 BCL11A Haploinsufficiency Causes an Intellectual Disability Syndrome and Dysregulates Transcription.
PMID 30250039
2018 Functional characterization of TBR1 variants in neurodevelopmental disorder.