Keratan and heparan sulphaturia: a mucopolysaccharidosis with an enzyme defect not previously identified

Reuben Matalon, R. Wappner, M. Deanching, I. K. Brandt, A. Horwitz

Research output: Contribution to journalArticle

2 Citations (Scopus)
Original languageEnglish (US)
Pages (from-to)57-58
Number of pages2
JournalJournal of Inherited Metabolic Disease
Volume5
Issue number1 Supplement
DOIs
StatePublished - Mar 1982
Externally publishedYes

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Mucopolysaccharidoses
Enzymes

ASJC Scopus subject areas

  • Genetics(clinical)
  • Genetics
  • Endocrinology

Cite this

Keratan and heparan sulphaturia : a mucopolysaccharidosis with an enzyme defect not previously identified. / Matalon, Reuben; Wappner, R.; Deanching, M.; Brandt, I. K.; Horwitz, A.

In: Journal of Inherited Metabolic Disease, Vol. 5, No. 1 Supplement, 03.1982, p. 57-58.

Research output: Contribution to journalArticle

Matalon, Reuben ; Wappner, R. ; Deanching, M. ; Brandt, I. K. ; Horwitz, A. / Keratan and heparan sulphaturia : a mucopolysaccharidosis with an enzyme defect not previously identified. In: Journal of Inherited Metabolic Disease. 1982 ; Vol. 5, No. 1 Supplement. pp. 57-58.
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