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Screening for Familial APP Mutations in Sporadic Cerebral Amyloid Angiopathy

Alessandro Biffi, Anna Plourde,  [ ... ], Jonathan Rosand

Comprehensive Approach to Analyzing Rare Genetic Variants

Thomas J. Hoffmann, Nicholas J. Marini, John S. Witte

A General Model of Codon Bias Due to GC Mutational Bias

Gareth A. Palidwor, Theodore J. Perkins, Xuhua Xia

Molecular Diagnosis of Neonatal Diabetes Mellitus Using Next-Generation Sequencing of the Whole Exome

Amélie Bonnefond, Emmanuelle Durand,  [ ... ], Philippe Froguel

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