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Zhang, X. et al. (n.d.). Mutations of PQBP1 in Renpenning syndrome promote ubiquitin-mediated degradation of FMRP and cause synaptic dysfunction. Human molecular genetics. pp. 955-968. [Online].
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Zhang, X. et al. (n.d.). Mutations of PQBP1 in Renpenning syndrome promote ubiquitin-mediated degradation of FMRP and cause synaptic dysfunction. Human molecular genetics. pp. 955-968. [Online].