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Search from 250 M+ research papersSearch from 250 M+ research papershttps://doi.org/10.1111/j.1365-2265.2008.03475.x
Copy DOI Journal: Clinical Endocrinology |  Publication Date: Jul 6, 2009 |
 Citations: 2 |
Affiliation: Semmelweis University, Hungarian Academy of SciencesUncommon MEN2A phenotype in a patient with a RET protooncogene exon 10, codon 611 mutation
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