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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
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1990 | 1 |
1991 | 1 |
1996 | 1 |
2024 | 0 |
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Schindler disease: the molecular lesion in the alpha-N-acetylgalactosaminidase gene that causes an infantile neuroaxonal dystrophy.
J Clin Invest. 1990 Nov;86(5):1752-6. doi: 10.1172/JCI114901.
J Clin Invest. 1990.
PMID: 2243144
Free PMC article.
Lysosomal alpha-N-acetylgalactosaminidase deficiency, the enzymatic defect in angiokeratoma corporis diffusum with glycopeptiduria.
Kanzaki T, Wang AM, Desnick RJ.
Kanzaki T, et al.
J Clin Invest. 1991 Aug;88(2):707-11. doi: 10.1172/JCI115357.
J Clin Invest. 1991.
PMID: 1907616
Free PMC article.
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Fabry disease: fourteen alpha-galactosidase A mutations in unrelated families from the United Kingdom and other European countries.
Davies JP, Eng CM, Hill JA, Malcolm S, MacDermot K, Winchester B, Desnick RJ.
Davies JP, et al.
Eur J Hum Genet. 1996;4(4):219-24. doi: 10.1159/000472202.
Eur J Hum Genet. 1996.
PMID: 8875188
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