chromosomal translocation t2q11:15q21

chromosomal translocation t(2;15)(q11;q21) involving DYX1C1 may be a cause of dyslexia

Properties

GENERAL: chromosomal translocation FORM: t2q11:15q21 LOCUS: human chromosome-2 Q11 human chromosome-15 Q21 PATHOLOGY: dyslexia

References

UniProt :accession Q8WXU2