Articles with "mutation familial" as a keyword



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A novel DICER1 mutation in familial multinodular goitre

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Published in 2018 at "Clinical Endocrinology"

DOI: 10.1111/cen.13613

Abstract: Multinodular goitre (MNG) is a common disease, present in 20% of the general population. It is more frequent in females, elderly patients, and low iodine regions. Genetically linked loci for familial MNG were found on… read more here.

Keywords: mutation familial; dicer1 mutation; multinodular goitre; goitre ... See more keywords