A study of the renal handling and intestinal absorption of dibasic amino acids in a patient with genotype +/11 heterozygous cystinuria and idiopathic hypercalcuria
Author:
Publisher
Elsevier BV
Subject
Biochemistry (medical),Clinical Biochemistry,Biochemistry,General Medicine
Reference21 articles.
1. Disorders of intestinal amino-acid transport
2. Disorders of intestinal amino-acid transport
3. PHENOTYPES AND GENOTYPES IN CYSTINURIA
4. THE PATTERN OF AMINO-ACID EXCRETION IN CYSTINURIA
5. Cystinuria: biochemical evidence for three genetically distinct diseases.
Cited by 4 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献
1. The Spectrum of Metabolic Abnormalities in Patients with Cystine Nephrolithiasis;Journal of Urology;1989-04
2. Heterozygous cystinuria and urinary lithiasis;American Journal of Medical Genetics;1985-12
3. Some observations on genetic factors in urolithiasis;Urology;1981-01
4. Genetics of Cystinuria in an Inbred Population;Journal of Urology;1978-04
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