Work

In vitro read‐through of phenylalanine hydroxylase (PAH) nonsense mutations using aminoglycosides: a potential therapy for phenylketonuria

Year: 2013

Type: article

Source: Journal of Inherited Metabolic Disease

DOI: 10.1007/s10545-013-9602-6

Authors: Gladys Ho, Juergen Reichardt, John Christodoulou

Institutions: The University of Sydney, Children's Hospital at Westmead, James Cook University

Language: English

Topic: Metabolism and Genetic Disorders

Subfield: Clinical Biochemistry

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

OpenAlex ID: W2078054347

FWCI: 2.898

Cites: 35

Cited by: 21

Related to: 10