Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity (Q28268714)

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Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity
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    Wolcott-Rallison Syndrome: clinical, genetic, and functional study of EIF2AK3 mutations and suggestion of genetic heterogeneity (English)
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    Krishna M Vattem
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    Marc Delépine
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    Lynn A Rainbow
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    Céline Haton
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    Annick Lecoq
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    Nick J Shaw
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    Jean-Jacques Robert
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    Raoul Rooman
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    Catherine Diatloff-Zito
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    Bassan Bin-Abbas
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    Doris Taha
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    Bernard Zabel
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    Piergiorgio Franceschini
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    A Kemal Topaloglu
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    Marc Nicolino
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    Ronald C Wek
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    July 2004
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    53
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    7
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    1876-83
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