A novel mutation in the upstream open reading frame of the CDKN1B gene causes a MEN4 phenotype.
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PLoS Genet. 2013 Mar;9(3):e1003350. doi: 10.1371/journal.pgen.1003350. Epub 2013 Mar 21.
PLoS Genet. 2013.
PMID: 23555276
Free PMC article.