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Disruption of the ATP8A2 gene in a patient with a t(10;13) de novo balanced translocation and a severe neurological phenotype

✍ Scribed by Cacciagli, Pierre; Haddad, Marie-Reine; Mignon-Ravix, Cécile; El-Waly, Bilal; Moncla, Anne; Missirian, Chantal; Chabrol, Brigitte; Villard, Laurent


Book ID
109849226
Publisher
Nature Publishing Group
Year
2010
Tongue
English
Weight
304 KB
Volume
18
Category
Article
ISSN
1018-4813

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