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Familial autosomal recessive bestrophinopathy: identification of a novel variant in BEST1 gene and the specific metabolomic profile.

Panpan YeJia XuYueqiu LuoZhitao SuKe Yao
Published in: BMC medical genetics (2020)
We identified a novel disease-associated variant in the BEST1 gene as well as a disease-specific metabolic feature in familial ARB. Our findings helped improve the understanding of ARB mechanisms.
Keyphrases
  • genome wide
  • copy number
  • early onset
  • machine learning
  • genome wide identification
  • gene expression
  • intellectual disability
  • dna methylation
  • autism spectrum disorder