The Molecular Defect Leading to Fabry Disease: Structure of Human α-Galactosidase
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- 6 February 2004
- journal article
- research article
- Published by Elsevier in Journal of Molecular Biology
- Vol. 337 (2) , 319-335
- https://doi.org/10.1016/j.jmb.2004.01.035
Abstract
No abstract availableKeywords
This publication has 61 references indexed in Scilit:
- Analysis of splice‐site mutations of the α‐galactosidase A gene in Fabry diseaseClinical Genetics, 2003
- Glycosidase mechanismsCurrent Opinion in Chemical Biology, 2002
- Gapped BLAST and PSI-BLAST: a new generation of protein database search programsNucleic Acids Research, 1997
- [20] Processing of X-ray diffraction data collected in oscillation modePublished by Elsevier ,1997
- CLUSTAL W: improving the sensitivity of progressive multiple sequence alignment through sequence weighting, position-specific gap penalties and weight matrix choiceNucleic Acids Research, 1994
- The CCP4 suite: programs for protein crystallographyActa Crystallographica Section D-Biological Crystallography, 1994
- Crystallization and Preliminary X-ray Analysis of Human α-Galactosidase A ComplexJournal of Molecular Biology, 1994
- The identification of α-galactosidase B from human liver as an α-acetylgalactosaminidaseBiochemical and Biophysical Research Communications, 1977
- A general method applicable to the search for similarities in the amino acid sequence of two proteinsJournal of Molecular Biology, 1970
- Ein Beitrag zur Kenntniss der Purpura haemorrhagica nodularis (Purpura papulosa haemorrhagica Hebrae)Archives of Dermatological Research, 1898