LOWE'S SYNDROME: Absence of Amino Acid Transport Defect in Cultured Fibroblasts
Author:
Publisher
Wiley
Subject
General Medicine,Pediatrics, Perinatology, and Child Health
Link
http://onlinelibrary.wiley.com/wol1/doi/10.1111/j.1651-2227.1973.tb17073.x/fullpdf
Reference5 articles.
1. Transport of Amino Acids by Confluent and Nonconfluent 3T3 and Polyoma Virus-transformed 3T3 Cells Growing on Glass Cover Slips
2. Transport of dibasic amino acids, cystine, and tryptophan by cultured human fibroblasts: absence of a defect in cystinuria and Hartnup disease
3. Increased Uptake of Amino Acids and 2-Deoxy-D-Glucose by Virus-Transformed Cells in Culture
Cited by 2 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 Oculocerebrorenal Syndrome of Lowe;Advances in Pediatrics;1991
2. Glycine transport by cultured skin fibroblasts from a patient with isolated hyperglycinuria;Journal of Inherited Metabolic Disease;1980-12
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