Late onset form of mucopolysaccharidosis type I: Clinical aspect and biochemical characterization of residual α‐l‐iduronidase activity
- 1 December 1981
- journal article
- work in-progress
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 4 (1) , 171-172
- https://doi.org/10.1007/bf02263645
Abstract
No abstract availableKeywords
This publication has 8 references indexed in Scilit:
- Biochemical Discrimination of Hurler and Scheie SyndromesClinical Science, 1979
- Variant of iduronidase deficient mucopolysaccharidoses: further evidence for genetic heterogeneity.Journal of Medical Genetics, 1977
- α‐L‐iduronidase deficiency and possible Hurler‐Scheie genetic compoundNeurology, 1976
- The Iduronidase-Deficient Mucopolysaccharidoses: Clinical and Roentgenographic FeaturesPublished by American Academy of Pediatrics (AAP) ,1976
- Hurler/Scheie genetic compound (mucopolysaccharidosis IH/IS) in Japanese brothersClinical Genetics, 1974
- ALLELISM, NON-ALLELISM, AND GENETIC COMPOUNDS AMONG THE MUCOPOLYSACCHARIDOSESThe Lancet, 1972
- Quantitativer Suchtest zur Bestimmung saurer Mucopolysaccharide im UrinAlbrecht von Graefes Archiv für Ophthalmologie, 1969
- Filtering Operations for Glaucoma: A Comparative Study*American Journal of Ophthalmology, 1962