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Year | Number of Results |
---|---|
1998 | 2 |
2004 | 1 |
2010 | 1 |
2013 | 1 |
2024 | 0 |
PubMed for id: 6136320
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Wolfram gene (WFS1) mutation causes autosomal dominant congenital nuclear cataract in humans.
Eur J Hum Genet. 2013 Dec;21(12):1356-60. doi: 10.1038/ejhg.2013.52. Epub 2013 Mar 27.
Eur J Hum Genet. 2013.
PMID: 23531866
Free PMC article.
A tissue-specific atlas of mouse protein phosphorylation and expression.
Huttlin EL, Jedrychowski MP, Elias JE, Goswami T, Rad R, Beausoleil SA, Villén J, Haas W, Sowa ME, Gygi SP.
Huttlin EL, et al.
Cell. 2010 Dec 23;143(7):1174-89. doi: 10.1016/j.cell.2010.12.001.
Cell. 2010.
PMID: 21183079
Free PMC article.
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Endoplasmic reticulum stress and N-glycosylation modulate expression of WFS1 protein.
Yamaguchi S, Ishihara H, Tamura A, Yamada T, Takahashi R, Takei D, Katagiri H, Oka Y.
Yamaguchi S, et al.
Biochem Biophys Res Commun. 2004 Dec 3;325(1):250-6. doi: 10.1016/j.bbrc.2004.10.017.
Biochem Biophys Res Commun. 2004.
PMID: 15522226
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Diabetes insipidus, diabetes mellitus, optic atrophy and deafness (DIDMOAD) caused by mutations in a novel gene (wolframin) coding for a predicted transmembrane protein.
Strom TM, Hörtnagel K, Hofmann S, Gekeler F, Scharfe C, Rabl W, Gerbitz KD, Meitinger T.
Strom TM, et al.
Hum Mol Genet. 1998 Dec;7(13):2021-8. doi: 10.1093/hmg/7.13.2021.
Hum Mol Genet. 1998.
PMID: 9817917
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A gene encoding a transmembrane protein is mutated in patients with diabetes mellitus and optic atrophy (Wolfram syndrome).
Inoue H, Tanizawa Y, Wasson J, Behn P, Kalidas K, Bernal-Mizrachi E, Mueckler M, Marshall H, Donis-Keller H, Crock P, Rogers D, Mikuni M, Kumashiro H, Higashi K, Sobue G, Oka Y, Permutt MA.
Inoue H, et al.
Nat Genet. 1998 Oct;20(2):143-8. doi: 10.1038/2441.
Nat Genet. 1998.
PMID: 9771706
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