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Exome Sequencing and Functional Analysis Identifies BANF1 Mutation as the Cause of a Hereditary Progeroid Syndrome

✍ Scribed by Xose S. Puente; Victor Quesada; Fernando G. Osorio; Rubén Cabanillas; Juan Cadiñanos; Julia M. Fraile; Gonzalo R. Ordóñez; Diana A. Puente; Ana Gutiérrez-Fernández; Miriam Fanjul-Fernández; Nicolas Lévy; José M.P. Freije; Carlos López-Otín


Book ID
113423034
Publisher
American Society of Human Genetics
Year
2011
Tongue
English
Weight
922 KB
Volume
88
Category
Article
ISSN
0002-9297

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