Work

Large deletions in the phenylalanine hydroxylase gene as a cause of phenylketonuria in India

Year: 1997

Type: article

Source: Journal of Inherited Metabolic Disease

DOI: 10.1023/a:1005352725283

Authors: P. Guldberg, K. F. Henriksen, K. C. Mammen, H. L. Levy, F. Güttler

Institutions: Kennedy Center, Boston Children's Hospital, Harvard 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: W43918075

FWCI: 0.453

Cites: 2

Cited by: 10

Related to: 10