Homo sapiens mRNA for alpha-fetoprotein enhancer binding protein, comp - Nucleotide

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ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes. [J Med Genet. 2024]
ZFHX3 variants cause childhood partial epilepsy and infantile spasms with favourable outcomes.
He MF, Liu LH, Luo S, Wang J, Guo JJ, Wang PY, Zhai QX, He SL, Zou DF, Liu XR, et al. J Med Genet. 2024 Jun 20; 61(7):652-660. Epub 2024 Jun 20.
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability. [Am J Hum Genet. 2024]
Haploinsufficiency of ZFHX3, encoding a key player in neuronal development, causes syndromic intellectual disability.
Pérez Baca MDR, Jacobs EZ, Vantomme L, Leblanc P, Bogaert E, Dheedene A, De Cock L, Haghshenas S, Foroutan A, Levy MA, et al. Am J Hum Genet. 2024 Mar 7; 111(3):509-528. Epub 2024 Feb 26.
Interaction network of human early embryonic transcription factors. [EMBO Rep. 2024]
Interaction network of human early embryonic transcription factors.
Gawriyski L, Tan Z, Liu X, Chowdhury I, Malaymar Pinar D, Zhang Q, Weltner J, Jouhilahti EM, Wei GH, Kere J, et al. EMBO Rep. 2024 Mar; 25(3):1589-1622. Epub 2024 Jan 31.