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In vitro read-through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria
Ho, Gladys, Reichardt, Juergen, Christodoulou, JohnVolume:
36
Language:
english
Pages:
5
Journal:
Journal of Inherited Metabolic Disease
DOI:
10.1007/s10545-013-9602-6
Date:
November, 2013
File:
PDF, 213 KB
english, 2013