(Q48309364)
Statements
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Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia. (English)
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André Mégarbané
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Alessandra Pangrazio
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Eliane Chouery
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Joseph Maarawi
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Sandra Sabbagh
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Gérard Lefranc
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Cristina Sobacchi
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31 October 2012
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56
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1
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32-35
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Identifiers
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