A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, β-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency-Reference-Cited by-同舟云学术

A review of the clinical presentation and laboratory findings in two uncommon hereditary disorders of sulfur amino acid metabolism, β-mercaptolactate cysteine disulfideuria and sulfite oxidase deficiency

Published:1985-06 Issue:3 Volume:18 Page:139-142
ISSN:0009-9120
Container-title:Clinical Biochemistry
language:en
Short-container-title:Clinical Biochemistry

Author:

Crawhall J.C.

Publisher

Elsevier BV

Subject

Clinical Biochemistry,General Medicine

Reference29 articles.

1. Mental deficiency and a new amino aciduria;Ampola;Am J Dis Child,1969

2. Two-way separation of amino acids and other ninhydrin-reacting substances by high voltage electrophoresis followed by paper chromatography;Efron;Biochem J,1959

3. β-Mercaptolactate-cysteine disulfide: Analog of cysteine in the urine of a mentally retarded patient;Crawhall;Science,1968

4. β-Mercaptolactate-cysteine disulfide in the urine of a mentally retarded patient;Crawhall;Am J Dis Child,1969

5. Synthesis of the alpha-hydroxy analogues of S-benzylcysteine and cysteine;Hope;J Chem Sac, Section C,1970

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