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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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2001 | 1 |
2016 | 1 |
2019 | 1 |
2024 | 0 |
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Fabry disease: twenty novel alpha-galactosidase A mutations causing the classical phenotype.
J Hum Genet. 2001;46(4):192-6. doi: 10.1007/s100380170088.
J Hum Genet. 2001.
PMID: 11322659
Review.
Genotype: A Crucial but Not Unique Factor Affecting the Clinical Phenotypes in Fabry Disease.
Pan X, Ouyang Y, Wang Z, Ren H, Shen P, Wang W, Xu Y, Ni L, Yu X, Chen X, Zhang W, Yang L, Li X, Xu J, Chen N.
Pan X, et al.
PLoS One. 2016 Aug 25;11(8):e0161330. doi: 10.1371/journal.pone.0161330. eCollection 2016.
PLoS One. 2016.
PMID: 27560961
Free PMC article.
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Mutation spectrum of α-Galactosidase gene in Japanese patients with Fabry disease.
Kobayashi M, Ohashi T, Kaneshiro E, Higuchi T, Ida H.
Kobayashi M, et al.
J Hum Genet. 2019 Jul;64(7):695-699. doi: 10.1038/s10038-019-0599-z. Epub 2019 Apr 15.
J Hum Genet. 2019.
PMID: 30988410
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