| 1 | NAGA, SCHND1
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| Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency: no association with neuroaxonal dystrophy?
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| Bakker HD, de Sonnaville ML, Vreken P, Abeling NG, Groener JE, Keulemans JL, van Diggelen OP.
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| Eur J Hum Genet 9(2):91-6. 2001
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| 2 | CYP2D6, NAGA, SREBF2, TSG22C
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| Refinement of an ovarian cancer tumour suppressor gene locus on chromosome arm 22q and mutation analysis of CYP2D6, SREBP2 and NAGA.
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| Bryan EJ, Thomas NA, Palmer K, Dawson E, Englefield P, Campbell IG.
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| Int J Cancer 87(6):798-802. 2000
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| 3 | NAGA
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| Human alpha-N-acetylgalactosaminidase (alpha-NAGA) deficiency : new mutations and the paradox between genotype and phenotype.
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| Keulemans JLM, et al.
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| J Med Genet 33 : 458-464. 1996
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| 4 | NAGA, SCHND1
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| Neuroaxonal dystrophy in infantile alpha-N-acetylgalactosaminidase deficiency.
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| Wolfe DE, Schindler D, Desnick RJ.
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| J Neurol Sci 132(1):44-56. 1995
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| 5 | NAGA
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| The molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes angiokeratoma corporis diffusum with glycopeptiduria.
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| Wang AM, et al.
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| J Clin Invest 94 : 839-845. 1994
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| 6 | NAGA
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| BamHI polymorphism at N-acetyl-alpha-galactosaminidase locus (NAGA).
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| Yamauchi T, et al.
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| Nucleic Acids Res 19 : 2518. 1991
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| 7 | NAGA
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| Lysosomal alpha-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria.
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| Kanzaki T, et al.
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| J Clin Invest 88 : 707-711. 1991
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| 8 | NAGA
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| Human alpha-N-acetylgalactosaminidase-molecular cloning, nucleotide sequence, and expression of a full-length cDNA. Homology with human alpha-galactosidase A suggests evolution from a common ancestral gene.
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| Wang AM, Bishop DF, Desnick RJ.
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| J Biol Chem 265(35):21859-66. 1990
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| 9 | NAGA, SCHND1
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| Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy.
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| Wang AM, Schindler D, Desnick R.
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| J Clin Invest 86(5):1752-6. 1990
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| 10 | NAGA
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| Molecular cloning of a full-length cDNA for human alpha-N-acetylgalactosaminidase (alpha-galactosidase B).
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| Tsuji S, Yamauchi T, Hiraiwa M, Isobe T, Okuyama T, Sakimura K, Takahashi Y, Nishizawa M, Uda Y, Miyatake T.
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| Biochem Biophys Res Commun 163(3):1498-504. 1989
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| 11 | ATAD5, NAGA, SCHND1
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| Neuroaxonal dystrophy due to lysosomal alpha-N-acetylgalactosaminidase deficiency.
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| Schindler D, Bishop DF, Wolfe DE, Wang AM, Egge H, Lemieux RU, Desnick RJ.
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| N Engl J Med 320(26):1735-40. No abstract available. 1989
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| 12 | ATAD5, NAGA
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| Lysosomal alpha-N-acetylgalactosaminidase deficiency: a new inherited metabolic disease.
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| van Diggelen OP, Schindler D, Kleijer WJ, Huijmans JM, Galjaard H, Linden HU, Peter-Katalinic J, Egge H, Dabrowski U, Cantz M.
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| Lancet 2(8562):804. No abstract available. 1987
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| 13 | NAGA
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| Isolation of the human alpha-galactosidase A and B genes.
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| Myszkiewicz BA, et al.
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| Fed Proc 43 : 1529. 1984
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| 14 | NAGA
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| Regional localization of NAGA, and ACO2 on human chromosome 22.
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| Geurts van Kessel AHM, et al.
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| Cytogenet Cell Genet 25 : 161. 1979
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| 15 | NAGA
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| Localization of a gene for human alpha-galactosidase B (=N-acetyl-alpha-D-galactosaminidase) on chromosome 22.
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| de Groot PG, et al.
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| Hum Genet 44 : 305-312. 1978
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