Homocystinuria: Diagnosis and Management
Author:
Publisher
Springer International Publishing
Link
http://link.springer.com/content/pdf/10.1007/978-3-319-14621-8_14
Reference49 articles.
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2. Carson NA, Neill DW. Metabolic abnormalities detected in a survey of mentally backward individuals in Northern Ireland. Arch Dis Child. 1962;37:505–13.
3. Yannicelli S, et al. Improved growth and nutrition status in children with methylmalonic or propionic acidemia fed an elemental medical food. Mol Genet Metab. 2003;80(1–2):181–8.
4. Singh RH, et al. Recommendations for the nutrition management of phenylalanine hydroxylase deficiency. Genet Med. 2014;16(2):121–31.
5. Mudd SH, et al. Homocystinuria: an enzymatic defect. Science. 1964;143(3613):1443–5.
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