Work

Autosomal dominant GTP cyclohydrolase I (AD GCH 1) deficiency (Segawa disease, dystonia 5; DYT 5).

Year: 2009

Type: article

Source: PubMed

Author: Masaya Segawa

Institution: Segawa Neurological Clinic for Children

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: W170614698

FWCI: 2.598

Cites: 78

Cited by: 45

Related to: 10