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The R215W mutation in NBS1 impairs γ-H2AX binding and affects DNA repair: molecular bases for the severe phenotype of 657del5/R215W Nijmegen breakage syndrome patients

✍ Scribed by Alessandra di Masi; Mara Viganotti; Fabio Polticelli; Paolo Ascenzi; Caterina Tanzarella; Antonio Antoccia


Book ID
116296521
Publisher
Elsevier Science
Year
2008
Tongue
English
Weight
574 KB
Volume
369
Category
Article
ISSN
0006-291X

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