Work

Holocarboxylase synthetase deficiency: 9‐year follow‐up of a patient on chronic biotin therapy and a review of the literature

Year: 1988

Type: article

Study design: Case Report

Source: Journal of Inherited Metabolic Disease

DOI: 10.1007/bf01799223

Authors: A. J. Michalski, G. T. Berry, S. Segal

Institutions: Children's Hospital of Philadelphia, University of Pennsylvania

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: W2012305444

FWCI: 0.309

Cites: 20

Cited by: 21

Related to: 10