CISD2 wt Allele

Known as: Zinc Finger, CDGSH-Type Domain 2 Gene, CDGSH Iron Sulfur Domain 2 wt Allele, WFS2 
Human CISD2 wild-type allele is located in the vicinity of 4q24 and is approximately 24 kb in length. This allele, which encodes CDGSH iron-sulfur… (More)

Topic mentions per year

Topic mentions per year

2009-2017
012320092017

Papers overview

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2018
2018
Wolfram syndrome (WFS) is a rare autosomal premature aging syndrome that shows signs of diabetes mellitus, optic atrophy, and… (More)
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2017
2017
Wolfram syndrome (WFS) is a rare autosomal recessive disease with non-autoimmune childhood onset insulin dependent diabetes and… (More)
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2014
2014
Wolfram Syndrome type 2 (WFS2) is considered a phenotypic and genotypic variant of WFS, whose minimal criteria for diagnosis are… (More)
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Review
2010
Review
2010
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is an evolutionarily conserved novel gene. Recently, we have… (More)
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Highly Cited
2009
Highly Cited
2009
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Significantly, the CISD2… (More)
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2009
2009
The endoplasmic reticulum protein Miner1 is essential for health and longevity. Mis-splicing of CISD2, which codes for Miner1, is… (More)
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2009
2009
CISD2, the causative gene for Wolfram syndrome 2 (WFS2), is a previously uncharacterized novel gene. Using a mouse genetic… (More)
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