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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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2015 | 1 |
2016 | 1 |
2018 | 1 |
2024 | 0 |
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The spectrum of KIAA0196 variants, and characterization of a murine knockout: implications for the mutational mechanism in hereditary spastic paraplegia type SPG8.
Orphanet J Rare Dis. 2015 Nov 16;10:147. doi: 10.1186/s13023-015-0359-x.
Orphanet J Rare Dis. 2015.
PMID: 26572744
Free PMC article.
Expression of N471D strumpellin leads to defects in the endolysosomal system.
Song L, Rijal R, Karow M, Stumpf M, Hahn O, Park L, Insall R, Schröder R, Hofmann A, Clemen CS, Eichinger L.
Song L, et al.
Dis Model Mech. 2018 Sep 13;11(9):dmm033449. doi: 10.1242/dmm.033449.
Dis Model Mech. 2018.
PMID: 30061306
Free PMC article.
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Loss of strumpellin in the melanocytic lineage impairs the WASH Complex but does not affect coat colour.
Tyrrell BJ, Woodham EF, Spence HJ, Strathdee D, Insall RH, Machesky LM.
Tyrrell BJ, et al.
Pigment Cell Melanoma Res. 2016 Sep;29(5):559-71. doi: 10.1111/pcmr.12506.
Pigment Cell Melanoma Res. 2016.
PMID: 27390154
Free PMC article.
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