| 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 | 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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| 3 | 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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| 4 | 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
|