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Article

Uncommon MEN2A phenotype in a patient with a RET protooncogene exon 10, codon 611 mutation.

Clinical endocrinology - 1 Aug 2009

Igaz Peter, Patócs Attila, Rácz Károly

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Methodology Data sources Editorial policy Privacy About Contact Helena Bioinformatics

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Source

Identifiers

PMID: 19018781
DOI: 10.1111/j.1365-2265.2008.03475.x

Genes

RET

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PubMed metadata and Literature Corpus relationships. Corpus snapshot updated 7 Sept 2026.

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