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Wolcott-Rallison syndrome - Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity

Publié le 6 octobre 2017
Wolcott-Rallison syndrome - Clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity
Description
 
Auteurs
Senee V, Vattem KM, Delepine M, Rainbow LA, Haton C, Lecoq A, Shaw NJ, Robert JJ, Rooman R, Diatloff-Zito C, Michaud JL, Bin-Abbas B, Taha D, Zabel B, Franceschini P, Topaloglu AK, Lathrop GM, Barrett TG, Nicolino M, Wek RC and Julier C
Revue
Diabetes 53 (7), 1876-1883, 2004
Année2 004
Service
IG/CNG
Institut
 
Laboratoire
 
Date de création06/01/2017
Facteur Impact 

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