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TTC8 gene

Known as: TETRATRICOPEPTIDE REPEAT DOMAIN-CONTAINING PROTEIN 8, BBS8, TTC8 
 
National Institutes of Health

Papers overview

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2019
2019
  • Lin Sun, Junmin Pan
  • Sheng wu gong cheng xue bao = Chinese journal of…
  • 2019
  • Corpus ID: 73428203
Cilia and flagella on eukaryotic cells are polarized organelles extending from the surfaces of cells, which participate not only… Expand
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2019
2019
Bardet–Biedl syndrome (BBS), characterized by rod-cone dystrophy, postaxial polydactyly, central obesity, hypogonadism, renal… Expand
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2016
2016
Nonsyndromic retinitis pigmentosa (RP) is genetically highly heterogeneous, with >100 disease genes identified. However… Expand
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2016
2016
Ciliary genes FAM161A and TTC8 have been implicated in retinal degeneration (RD) in humans and in dogs. The identification of… Expand
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2009
2009
Bardet Biedl syndrome is a genetically heterogeneous ciliopathy with fourteen genes currently identified. To date, mutations in… Expand
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2006
2006
AbstractBBS8 is one of the eight genes identified to date for Bardet-Biedl syndrome (BBS)—an autosomal recessive condition… Expand
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