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Published in 2020 at "Stem cell research"
DOI: 10.1016/j.scr.2020.101873
Abstract: Wilson's disease (WD) is an inherited autosomal recessive disease, which is caused by the mutation of ATP7B gene encoding copper-transporting ATPase protein. The WD patients always suffer from the excessive copper deposition in the liver…
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Keywords:
atp7b gene;
disease;
stem cell;
induced pluripotent ... See more keywords