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Year | Number of Results |
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1997 | 1 |
2017 | 1 |
2019 | 1 |
2020 | 1 |
2024 | 0 |
PubMed (OMIM) for id: 10311
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VPS26C homozygous nonsense variant in two cousins with neurodevelopmental deficits, growth failure, skeletal abnormalities, and distinctive facial features.
Clin Genet. 2020 Apr;97(4):644-648. doi: 10.1111/cge.13690. Epub 2019 Dec 26.
Clin Genet. 2020.
PMID: 31845315
Retriever is a multiprotein complex for retromer-independent endosomal cargo recycling.
McNally KE, Faulkner R, Steinberg F, Gallon M, Ghai R, Pim D, Langton P, Pearson N, Danson CM, Nägele H, Morris LL, Singla A, Overlee BL, Heesom KJ, Sessions R, Banks L, Collins BM, Berger I, Billadeau DD, Burstein E, Cullen PJ.
McNally KE, et al.
Nat Cell Biol. 2017 Oct;19(10):1214-1225. doi: 10.1038/ncb3610. Epub 2017 Sep 11.
Nat Cell Biol. 2017.
PMID: 28892079
Free PMC article.
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Isolation of a novel human gene from the Down syndrome critical region of chromosome 21q22.2.
Nakamura A, Hattori M, Sakaki Y.
Nakamura A, et al.
J Biochem. 1997 Oct;122(4):872-7. doi: 10.1093/oxfordjournals.jbchem.a021835.
J Biochem. 1997.
PMID: 9399594
Free article.
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