Labonne, J.D., Lee, K.H., Iwase, S., Kong, I.K., Diamond, M.P., Layman, L.C., Kim, C.H., Kim, H.G. (2016) An atypical 12q24.31 microdeletion implicates six genes including a histone demethylase KDM2B and a histone methyltransferase SETD1B in syndromic intellectual disability. Human genetics. 135(7):757-71
Additional Citations (1):
ZFIN Staff (2003) Curation of orthology data. Manually curated data.
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