C8orf37 gene

Known as: RP64, C8orf37, FLJ30600 
 
National Institutes of Health

Topic mentions per year

Topic mentions per year

2013-2016
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Papers overview

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2016
2016
PURPOSE More than 50 genes are reported as causative genes of autosomal recessive (ar) retinitis pigmentosa (RP) and cone-rod… (More)
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2016
2016
Bardet-Biedl syndrome (BBS) is a pleiotropic and clinically and genetically heterogeneous ciliopathy. Primary features are early… (More)
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2016
2016
BACKGROUND To identify the disease-causing mutation in a consanguineous family of Morrocan origin with syndromic autosomal… (More)
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2013
2013
PURPOSE To provide the clinical features in patients with retinal disease caused by C8orf37 gene mutations. METHODS Eight… (More)
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