A rationale for cystine supplementation in severe homocystinuria
Author:
Publisher
Wiley
Subject
Genetics(clinical),Genetics
Link
http://www.springerlink.com/index/pdf/10.1007/s10545-006-0452-3
Reference9 articles.
1. Briddon A (1998) Total plasma homocysteine as part of the routine aminogram by ion-exchange chromatography. Amino Acids 15: 235–239.
2. Briddon A (2003) Observations on albumin-aminothiol binding. J Inherit Metab Dis 26(Supplement 1): 51.
3. Fowler B (1997) Disorders of homocysteine metabolism. J Inherit Metab Dis 20: 731–741.
4. Hargreaves IP, Lee PJ, Briddon A (2002) Homocysteine and cysteine-albumin binding in homocystinuria: assessment of cysteine status and implications for glutathione synthesis? Amino Acids 22: 109–118.
5. Moat SJ, Bonham JR, Tanner MS, Allen JC, Powers HJ (1995) Recommended approaches for the laboratory measurement of homocysteine in the diagnosis and monitoring of patients with hyperhomocysteinaemia. Ann Clin Biochem 36: 372–379.
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