Cite
HARVARD Citation
Chen, H. et al. (2018). An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease. European journal of human genetics. pp. 1810-1818. [Online].
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Chen, H. et al. (2018). An MTF1 binding site disrupted by a homozygous variant in the promoter of ATP7B likely causes Wilson Disease. European journal of human genetics. pp. 1810-1818. [Online].