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CABP4 gene

Known as: CABP4, calcium binding protein 4, CSNB2B 
National Institutes of Health

Papers overview

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2018
2018
Leber congenital amaurosis (LCA) is a heterogeneous infantile retinal dystrophy presenting with severe visual loss, nystagmus… 
2014
2014
  • 2014
  • Corpus ID: 207766993
Dear Editor: I read with interest the analysis of Dutch patients diagnosed with congenital stationary night blindness (CSNB) by… 
2010
2010
PURPOSE. Congenital stationary night blindness (CSNB) is a clinically and genetically heterogeneous retinal disease. Although… 
2005
2005
CONCLUSIONS. Results indicate that the cone synaptic function in Cabp4Gnat1 mice was severely disrupted, whereas the morphologic…