Iminopeptiduria, skin ulcerations, and edema in a boy with prolidase deficiency

Author:

Sheffield Leslie J.,Schlesinger Peter,Faull Kym,Halpern Bert J.,Schier Garry M.,Cotton Richard G.H.,Hammond Judith,Danks David M.

Publisher

Elsevier BV

Subject

Pediatrics, Perinatology and Child Health

Reference13 articles.

1. A prolidase deficiency in man with iminopeptiduria;Powell;Metabolism,1974

2. Iminopeptiduria: A genetic defect in recycling collagen; a method for determining prolidase in erythrocytes;Jackson;Can Med Assoc J,1975

3. A syndrome resembling lathyrism associated with iminodipeptiduria;Goodman;Am J Med,1968

4. Further studies on a patient with iminopeptiduria: a probable case of prolidase deficiency;Buist;Metabolism,1972

5. Screening for aminoaciduria, a critical evaluation of four techniques and a survey of a mentally retarded population;Tippett;Aust Paediatr J,1972

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