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LRP5 BIALLELIC MUTATIONS CAUSE A HIGHER INCIDENCE OF SEVERE PHENOTYPE COMPARED WITH LRP5 MONOALLELIC MUTATION.

Chunli ChenXiang ZhangXiao-Yan PengFeng HuYizhe ChengPeiquan Zhao
Published in: Retina (Philadelphia, Pa.) (2022)
The severity of phenotype was more likely to be related to the synergistic effect of the variants.
Keyphrases
  • risk factors
  • intellectual disability
  • early onset
  • low density lipoprotein
  • cancer therapy
  • drug induced
  • autism spectrum disorder
  • dna methylation