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Homozygous stop mutation in the SNX10 gene in a consanguineous Iraqi boy with osteopetrosis and corpus callosum hypoplasia

✍ Scribed by Mégarbané, André; Pangrazio, Alessandra; Villa, Anna; Chouery, Eliane; Maarawi, Joseph; Sabbagh, Sandra; Lefranc, Gérard; Sobacchi, Cristina

Book ID
123600597
Publisher
Elsevier Science
Year
2013
Tongue
English
Weight
553 KB
Volume
56
Category
Article
ISSN
1769-7212

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