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https://pubmed.ncbi.nlm.nih.gov/9890194/ Molecular mechanisms of copper metabolism and the role of the Menkes disease protein Menkes disease is an X-linked, recessive disorder of copper metabolism that occurs in approximately 1 in 200,000 live births. The condition is characterized by... and the menkes disease molecular mechanisms copper https://www.nyp.org/pediatrics/genetics/menkes Menkes Disease - Genetics - Pediatrics | NewYork-Presbyterian menkes disease genetics pediatrics newyork presbyterian https://medlineplus.gov/ency/article/001160.htm Menkes disease: MedlinePlus Medical Encyclopedia Menkes disease is a genetic disorder in which the body has a problem absorbing and distributing copper to bodily organs. The disease affects mental and... menkes disease medlineplus medical encyclopedia https://www.wikidata.org/wiki/Q28269062 Isolation of a candidate gene for Menkes disease that encodes a potential heavy metal binding... https://pmc.ncbi.nlm.nih.gov/articles/PMC42272/ The Menkes/Wilson disease gene homologue in yeast provides copper to a ceruloplasmin-like oxidase... The CCC2 gene of the yeast Saccharomyces cerevisiae is homologous to the human genes defective in Wilson disease and Menkes disease. A biochemical hallmark of...