A Population-Based Genomic Study of Inherited Metabolic Diseases Detected Through Newborn Screening. [electronic resource]
Producer: 20170207Description: 561-72 p. digitalISSN:- 2234-3814
- Computational Biology
- DNA -- chemistry
- Dried Blood Spot Testing
- Galactokinase
- Genomics
- Haplotypes
- High-Throughput Nucleotide Sequencing
- Humans
- Incidence
- Infant, Newborn
- Membrane Proteins -- genetics
- Metabolic Diseases -- diagnosis
- Metabolism, Inborn Errors -- diagnosis
- Mitochondrial Membrane Transport Proteins -- genetics
- Neonatal Screening
- Polymorphism, Genetic
- Republic of Korea -- epidemiology
- Sequence Analysis, DNA
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Publication Type: Journal Article
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