Title : Multiple neoplasia in a patient with Gitelman syndrome harboring germline monoallelic MUTYH mutation.

Pub. Date : 2020

PMID : 33024574






1 Functional Relationships(s)
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1 We postulate that monoallelic MUTYH mutations may manifest in the presence of cooperative non-genetic mechanisms, in this case possibly magnesium deficiency from Gitelman syndrome. Magnesium mutY DNA glycosylase Homo sapiens