Hydroxyprolinemia: Comparison of a patient and her unaffected twin sister
- 31 March 1997
- journal article
- case report
- Published by Elsevier in The Journal of Pediatrics
- Vol. 130 (3) , 437-441
- https://doi.org/10.1016/s0022-3476(97)70207-5
Abstract
No abstract availableKeywords
This publication has 10 references indexed in Scilit:
- Newborn urine screening experience with over one million infants in the Quebec Network of Genetic MedicineJournal of Inherited Metabolic Disease, 1987
- Urine screening for aminoacidopathies: Is it beneficial?The Journal of Pediatrics, 1980
- Hydroxyprolinaemia with normal development.Archives of Disease in Childhood, 1980
- Newborn Urine ScreeningPublished by Springer Nature ,1980
- Hydroxyproline Metabolism in Two Sisters with HydroxyprolinemiaHuman Heredity, 1979
- Hydroxyprolinemia as an Illustration of Nonessential Enzymes in ManNew England Journal of Medicine, 1970
- Hydroxyprolinemia* an Apparently Harmless Familial Metabolic DisorderNew England Journal of Medicine, 1970
- Hydroxyprolinemia III. The origin of free hydroxyproline in hydroxyprolinemia. Collagen turnover. Evidence for a biosynthetic pathway in manBiochimica et Biophysica Acta (BBA) - General Subjects, 1968
- HydroxyprolinemiaNew England Journal of Medicine, 1965
- Hydroxyprolinemia Associated with Mental DeficiencyNew England Journal of Medicine, 1962