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Dive into the research topics of 'Wolcott-Rallison syndrome: Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity'. Together they form a unique fingerprint.- Sort by
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Valérie Senée, Krishna M. Vattem, Marc Delépine, Lynn A. Rainbow, Céline Haton, Annick Lecoq, Nick J. Shaw, Jean Jacques Robert, Raoul Rooman, Catherine Diatloff-Zito, Jacques L. Michaud, Bassan Bin-Abbas, Doris Taha, Bernard Zabel, Piergiorgio Franceschini, A. Kemal Topaloglu, G. Mark Lathrop, Timothy G. Barrett, Marc Nicolino, Ronald C. Wek
Research output: Contribution to journal › Article › peer-review