Inborn Errors of Proline Metabolism
Author:
Publisher
Oxford University Press (OUP)
Subject
Nutrition and Dietetics,Medicine (miscellaneous)
Link
http://academic.oup.com/jn/article-pdf/138/10/2016S/23902279/2016s.pdf
Reference51 articles.
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2. Disorders of proline and hydroxyproline metabolism;Phang,2001
3. A human homologue of the Drosophila melanogaster sluggish-A (proline oxidase) gene maps to 22q11.2, and is a candidate gene for type-I hyperprolinaemia;Campbell;Hum Genet.,1997
4. Association of hyperprolinaemia type I and heparin cofactor II deficiency with CATCH 22 syndrome: evidence for a contiguous gene syndrome locating the proline oxidase gene;Jaeken;J Inherit Metab Dis.,1996
5. Hyperprolinaemia and hereditary nephritis;Kopelman;Lancet.,1964
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