Newborn Screening in Japan-2021
- PMID: 35076455
- PMCID: PMC8788497
- DOI: 10.3390/ijns8010003
Newborn Screening in Japan-2021
Abstract
Japan's Newborn Mass Screening (NBS) was started in 1977 for amino acid metabolism disorders (phenylketonuria (PKU), homocystinuria, maple syrup urine, histidineemia (discontinued in 1993)) and galactosemia at the national level as a national project [...].
Conflict of interest statement
The author declares no conflict of interest.
References
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- Shino O., Daijiro K., Shogo T., Satoshi K., Tomoko S., Noriko N., Kouji Y., Haruo S., Takashi H. Clinical and Genetic Characteristics of Patients with Mild Hyperphenylalaninemia Identified by Newborn Screening Program in Japan. Int. J. Neonatal Screen. 2021;7:17. doi: 10.3390/ijns7010017. - DOI - PMC - PubMed
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