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SDCCAG8 gene

Known as: SDCCAG8, SLSN7, NPHP10 
 
National Institutes of Health

Papers overview

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2016
2016
Recessive mutations in the SDCCAG8 gene cause a nephronophthisis-related ciliopathy with Bardet-Biedl syndrome-like features in… Expand
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2015
2015
Apolipoprotein L1 ( APOL1 )-associated nephropathies comprise a spectrum of related nondiabetic kidney diseases strongly… Expand
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2014
2014
Nephronophthisis-related ciliopathies (NPHP-RCs) are developmental and degenerative kidney diseases that are frequently… Expand
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2014
2014
Mutations of SDCCAG8 are associated with nephronophthisis and Bardet-Biedl syndrome, as well as schizophrenia; however, the… Expand
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2012
2012
Genome-wide association analyses (GWAS) contributed to the detection of a number of single-nucleotide polymorphisms (SNPs… Expand
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Highly Cited
2011
Highly Cited
2011
Nephronophthisis (NPHP), an autosomal recessive cystic kidney disease, is the most frequent genetic cause for end-stage renal… Expand
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Highly Cited
2010
Highly Cited
2010
Nephronophthisis-related ciliopathies (NPHP-RC) are recessive disorders that feature dysplasia or degeneration occurring… Expand
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Highly Cited
2010
Highly Cited
2010
The ciliopathies are an expanding group of disorders caused by mutations in genes implicated in the biogenesis and function of… Expand
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2005
2005
From pea plants (Pisum sativum) with necrotic stem streaking a virus (E207) was isolated and readily transmitted by sap to all 30… Expand
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