Journal of Inborn Errors of Metabolism and Screening : Impact Factor & More
eISSN: 2326-4594pISSN: 2326-4098
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Key Metrics
CiteScore 
1.1
H-Index
12
SJR
Q3Genetics (clinical)
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Topics Covered on Journal of Inborn Errors of Metabolism and Screening
Journal of Inborn Errors of Metabolism and Screening Journal Specifications
Indexed in the following public directories
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SJR
| Overview | |
| Publisher | Latin American Society Inborn Errors and Neonatal Screening |
| Language | English |
| Article Processing Charges | USD 400 |
| Publication Time | 12 |
| Editorial Review Process | Anonymous peer review |
| General Details | |
| Language | English |
| Society/Institute/Sponsor | Latin American Society Inborn Errors and Neonatal Screening |
| Website URL | Visit website |
| Publication Details | |
| Editorial Review Detail | |
| Information for authors | |
| Author instructions | Visit website |
| Copyright Details | Visit website |
| Deposit Policy | Sherpa/Romeo |
| License type | CC BY |
| OA statement | Visit website |
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Recently Published Papers in Journal of Inborn Errors of Metabolism and Screening
Recent Trends in the Incidence of Cystic Fibrosis in Paraguay: Analysis of the Period 2018-2023
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DNA Methylation Analysis and Phenotype Severity in Fabry Disease
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Fabry Disease: An Update Based on Evidence and Experience
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Recent Trends in the Incidence of Cystic Fibrosis in Paraguay: Analysis of the Period 2018-2023
- 1 Jan 2025
- Journal of Inborn Errors of Metabolism and Screening
Chronic and Variable Manifestations of Ornithine Transcarbamylase Deficiency in Heterozygous Carriers: A Case Series of Three Colombian Patients
- 1 Jan 2025
- Journal of Inborn Errors of Metabolism and Screening
Importance of Long-Term Follow-Up in the Prognosis of Mucopolysaccharidosis IV-A: A Case Report from Southwestern of Colombia
- 1 Jan 2025
- Journal of Inborn Errors of Metabolism and Screening
Casuistic Use of High-Dose Methylprednisolone in a Child with Acute Encephalopathy due to Metabolic Crisis in HIBCH Deficiency
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DNA Methylation Analysis and Phenotype Severity in Fabry Disease
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