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IQCB1 gene

Known as: SLSN5, KIAA0036, IQ MOTIF-CONTAINING PROTEIN B1 
 
National Institutes of Health

Papers overview

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2013
2013
PURPOSE To identify the causative mutations in two early-onset canine retinal degenerations, crd1 and crd2, segregating in the… Expand
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2013
2013
Mutations in the human NPHP5 gene cause retinal and renal disease, but the precise mechanism by which NPHP5 functions is not… Expand
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Highly Cited
2011
Highly Cited
2011
Leber congenital amaurosis (LCA), a severe autosomal recessive childhood blindness, is caused by mutations in at least 15 genes… Expand
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2011
2011
It has been well documented that mutations in the same retinal disease gene can result in different clinical phenotypes due to… Expand
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2011
2011
OBJECTIVE To investigate whether mutations in NPHP5 can cause Leber congenital amaurosis (LCA) without early-onset renal disease… Expand
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2008
2008
Nephronophthisis (NPHP) is an autosomal recessive cystic kidney disease, caused by mutations of at least nine different genes… Expand
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2006
2006
A series of new cationic iridium(III) complexes [Ir(piq)2(N/\N)]+PF6- (1-6) (piq =1-phenyl-isoquinoline) containing N/\N ligands… Expand
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Highly Cited
2005
Highly Cited
2005
Nephronophthisis (NPHP) is the most frequent genetic cause of chronic renal failure in children. Identification of four genes… Expand
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2005
2005
Genes encoding multiple IQ-motif proteins have been identified in the human genome and may be regulated by calmodulin (CaM… Expand
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1998
1998
Substantial verbal IQ (VIQ)-performance IQ (PIQ) discrepancies may reflect brain dysfunction. The authors examined 159 patients… Expand
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