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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… Expand
National Institutes of Health

Papers overview

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2017
2017
Wolfram syndrome (WFS) is a rare autosomal recessive disease with non-autoimmune childhood onset insulin dependent diabetes and… Expand
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2015
2015
Most patients with Wolfram syndrome carry mutations in WFS1, while a lower percentage present a mutation in CISD2 (also known as… Expand
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2014
2014
BackgroundWolfram Syndrome type 2 (WFS2) is considered a phenotypic and genotypic variant of WFS, whose minimal criteria for… Expand
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2014
2014
NAF-1 is an important [2Fe-2S] NEET protein associated with human health and disease. A mis-splicing mutation in NAF-1 results in… Expand
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2012
2012
Nutrient-deprivation autophagy factor-1 (NAF-1) was identified as an endoplasmic reticulum (ER) BCL-2-interacting protein, which… Expand
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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… Expand
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2010
2010
Genetic Predisposition for Type 1 Diabetes Mellitus - The Role of Endoplasmic Reticulum Stress in Human Disease Etiopathogenesis… Expand
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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… Expand
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Highly Cited
2007
Highly Cited
2007
A single missense mutation was identified in a novel, highly conserved zinc-finger gene, ZCD2, in three consanguineous families… Expand
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2002
2002
Wolfram syndrome is an autosomal recessive disorder with probable locus heterogeneity. Only insulin-dependent diabetes mellitus… Expand
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