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American Journal of Human Genetics|November 1, 1981
Feline mucopolysaccharidosis VI: purification and characterization of the resident arylsulfatase B activityD T Vine, M M McGovern, M E Haskins, et al.
The Journal of Biological Chemistry|November 10, 1982
Purification and properties of feline and human arylsulfatase B isozymes. Evidence for feline homodimeric and human monomeric structuresM M McGovern, D T Vine, M E Haskins, et al.
The Journal of Clinical Investigation|July 1, 1981
Characterization of the porphobilinogen deaminase deficiency in acute intermittent porphyria. Immunologic evidence for heterogeneity of the genetic defectP M Anderson, R M Reddy, K E Anderson, et al.
Annals of Human Genetics|May 1, 1982
Assignment of the gene for cytosolic alanine aminotransferase (AAT1) to human chromosome 8K H Astrin, F X Arredondo-Vega, R J Desnick, et al.
American Journal of Human Genetics|April 1, 1992
Mucopolysaccharidosis type VI: identification of three mutations in the arylsulfatase B gene of patients with the severe and mild phenotypes provides molecular evidence for genetic heterogeneityW D Jin, C E Jackson, R J Desnick, et al.
Surgery, Gynecology & Obstetrics|June 1, 1978
Clinical and experimental transplantation in enzymatic deficiency diseaseA J Matas, R J Desnick, J S Najarian, et al.
No to Hattatsu = Brain and Development|May 1, 1990
[Partial deletion of alpha-galactosidase A gene in a Japanese mutant of Fabry disease]H Sakuraba, D F Bishop, T Suzuki, et al.
Journal of Child Neurology|August 24, 1999
Cerebral glucose metabolism in type I alpha-N-acetylgalactosaminidase deficiency: an infantile neuroaxonal dystrophyJ Rudolf, M Grond, D Schindler, et al.
Science (New York, N.Y.)|August 30, 1996
Pycnodysostosis, a lysosomal disease caused by cathepsin K deficiencyB D Gelb, G P Shi, H A Chapman, et al.
Molecular Genetics and Metabolism|October 27, 1998
Murine alpha-N-acetylgalactosaminidase: isolation and expression of a full-length cDNA and genomic organization: further evidence of an alpha-galactosidase gene familyA M Wang, Y A Ioannou, K M Zeidner, et al.
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