Guidelines for diagnosis, treatment and management of urea cycle disorders in China.
10.3760/cma.j.cn112140-20220412-00319
- Collective Name:Committee of Clinical Biochemical Genetics, Branch of Medical Genetic Physician, Chinese Medical Doctor Association;Subspecialty Group of Endocrinologic, Hereditary and Metabolic Diseases, the Society of Pediatrics, Chinese Medical Association;Division of Genetics and Metabolomics Child Diseases and Health Care Branch, Chinese Association for Maternal and Child Health;Division of Biochemistry and Metabolism, Medical Genetics Branch, Chinese Medical Association;China Alliance of Rare Disease
- Publication Type:Journal Article
- MeSH:
Humans;
Urea Cycle Disorders, Inborn/diagnosis*;
Ornithine Carbamoyltransferase Deficiency Disease/diagnosis*;
China
- From:
Chinese Journal of Pediatrics
2022;60(11):1118-1126
- CountryChina
- Language:Chinese
