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Year | Number of Results |
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2000 | 1 |
2004 | 1 |
2024 | 0 |
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A frameshift mutation in prominin (mouse)-like 1 causes human retinal degeneration.
Hum Mol Genet. 2000 Jan 1;9(1):27-34. doi: 10.1093/hmg/9.1.27.
Hum Mol Genet. 2000.
PMID: 10587575
Identification of novel Prominin-1/CD133 splice variants with alternative C-termini and their expression in epididymis and testis.
Fargeas CA, Joester A, Missol-Kolka E, Hellwig A, Huttner WB, Corbeil D.
Fargeas CA, et al.
J Cell Sci. 2004 Aug 15;117(Pt 18):4301-11. doi: 10.1242/jcs.01315.
J Cell Sci. 2004.
PMID: 15316084
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