Congenital lysinuria: A new inherited transport disorder of dibasic amino acids
Author:
Publisher
Elsevier BV
Subject
Pediatrics, Perinatology, and Child Health
Reference14 articles.
1. The metabolic basis of inherited disease,1966
2. Protein intolerance with deficient transport of basic amino acids;Perheentupa;Lancet,1965
3. Hyperdibasicaminoaciduria: An inherited disorder of amino acid transport;Whelan;Pediat. Res.,1968
4. Cystinuria: Biochemical evidence for three genetically distinct diseases;Rosenberg;J. Clin. Invest.,1966
5. Cystinuria: Genetic heterogeneity and allelism;Rosenberg;Science,1966
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1. Lysinuric protein intolerance caused by a homozygous SLC7A7 deletion and presented with hyperferritinemia and osteoporosis in two siblings;Molecular Genetics and Metabolism Reports;2023-12
2. Amino Acid Transport Across the Mammalian Intestine;Comprehensive Physiology;2018-12-13
3. Hyperexcretion of homocitrulline in a Malaysian patient with lysinuric protein intolerance;European Journal of Pediatrics;2013-01-29
4. Primary Inherited Aminoacidurias;Genetic Diseases of the Kidney;2009
5. Lysinuric protein intolerance, an autosomal recessive disease;Clinical Genetics;2008-04-23
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