Molecular defect of caprineN‐acetylglucosamine‐6‐sulphatase deficiency. A single base substitution creates a stop codon in the 5′‐region of the coding sequence
- 1 January 1995
- journal article
- Published by Wiley in Journal of Inherited Metabolic Disease
- Vol. 18 (1) , 96
- https://doi.org/10.1007/bf00711390
Abstract
No abstract availableThis publication has 2 references indexed in Scilit:
- A cDNA clone for human glucosamine-6-sulphatase reveals differences between arylsulphatases and non-arylsulphatasesBiochemical Journal, 1992
- N‐acetylglucosamine 6‐sulphatase deficiency in a Nubian goat: A model of Sanfilippo syndrome type D (mucopolysaccharidosis IIID)Journal of Inherited Metabolic Disease, 1992