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Wolcott-Rallison Syndrome: clinical, genetic and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity
V Senee, KM Vattem, M Delepine, Lynne Rainbow, C Haton, A Lecoq, Nicholas Shaw, JJ Robert, R Rooman, C Diatloff-Zito, JL Michaud, B Bin-Abbas, D Taha, B Zabel, P Franceschini, AK Topaloglu, GM Lathrop, Timothy Barrett, M Nicolino, RC Wek
Research output: Contribution to journal › Article
143
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(Scopus)