In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria Journal Articles Refereed uri icon

Overview

Published in

  • Journal of Inherited Metabolic Disease

Time

Date/time value

  • 2013

Identity

Digital Object Identifier (DOI)

  • 10.1007/s10545-013-9602-6

Additional Document Info

Parent Title

  • JOURNAL OF INHERITED METABOLIC DISEASE

Volume

  • 36

Issue

  • 6

Publisher

  • Kluwer Academic Publishers