Work

Dual gene defects involving δ‐aminolaevulinate dehydratase and coproporphyrinogen oxidase in a porphyria patient

Year: 2005

Type: article

Study design: Case Report

Source: British Journal of Haematology

DOI: 10.1111/j.1365-2141.2005.05852.x

Authors: Reiko Akagi, Rikako Inoue, Shikibu Muranaka, Tsuyoshi Tahara, Shigeru Taketani, Karl E. Anderson, John D. Phillips, Shigeru Sassa

Institutions: Okayama University, Okayama Prefectural University, Kyoto Institute of Technology, General Department of Preventive Medicine, The University of Texas Medical Branch at Galveston, University of Utah, Rockefeller University

Language: English

Topic: Porphyrin Metabolism and Disorders

Subfield: Molecular Biology

Field: Biochemistry, Genetics and Molecular Biology

Domain: Life Sciences

SDG: Good health and well-being

Open Access status: closed

Funders: National Institutes of Health, National Institute of General Medical Sciences, National Institute of Diabetes and Digestive and Kidney Diseases, National Center for Research Resources, NIH Clinical Center

Awards: G1210355380, G1214933801, G3613222656, G3663316755, Porphyrin biosynthesis in normal and disease states, G682434247, GENETICS AND DEVELOPMENT OF ERYTHROID HEME ENZYMES, General Clinical Research Center

OpenAlex ID: W2062230711

FWCI: 0.882

Cites: 16

Cited by: 28

Related to: 10