Associated Papers
Performance of Expanded Newborn Screening in Norway Supported by Post-Analytical Bioinformatics Tools and Rapid Second-Tier DNA Analyses.
Tangeraas T et al.
International Journal of Neonatal Screening, 2020
Profound biotinidase deficiency: a rare disease among native Swedes.
Ohlsson A et al.
Journal of Inherited Metabolic Disease, 2010
Analysis of mutations causing biotinidase deficiency.
Pindolia K et al.
Human Mutation, 2010
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