Three dimensional structural studies of α-N-acetylgalactosaminidase (α-NAGA) in α-NAGA deficiency (Kanzaki disease): different gene mutations cause peculiar structural changes in α-NAGAs resulting in different substrate specificities and clinical phenotypes-Reference-Cited by-同舟云学术

Three dimensional structural studies of α-N-acetylgalactosaminidase (α-NAGA) in α-NAGA deficiency (Kanzaki disease): different gene mutations cause peculiar structural changes in α-NAGAs resulting in different substrate specificities and clinical phenotypes

Published:2005-01 Issue:1 Volume:37 Page:15-20
ISSN:0923-1811
Container-title:Journal of Dermatological Science
language:en
Short-container-title:Journal of Dermatological Science

Author:

Kanekura Takuro,Sakuraba Hitoshi,Matsuzawa Fumiko,Aikawa Seiichi,Doi Hirofumi,Hirabayashi Yoshio,Yoshii Noriko,Fukushige Tomoko,Kanzaki Tamotsu

Publisher

Elsevier BV

Subject

Dermatology,Molecular Biology,Biochemistry

Reference12 articles.

1. Novel lysosomal glycoamino acid storage disease with angiokeratoma corporis diffusum;Kanzaki;Lancet,1989

2. Immunoelectron microscopic analysis of lysosomal deposits in α-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum;Kanda;J Dermatol Sci,2002

3. Isolation and characterization of major urinary amino acid O-glycosides and a dipeptide O-glycoside from a new lysosomal storage disorder (Kanzaki disease);Hirabayashi;J Biol Chem,1990

4. Lysosomal α-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria;Kanzaki;J Clin Invest,1991

5. A new case of α-N-acetylgalactosaminidase deficiency with angiokeratoma corporis diffusum, with Meniere's syndrome and without mental retardation;Kodama;Br J Dermatol,2001

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