Phenotype variation in two-locus mouse models of Hirschsprung disease: Tissue-specific interaction between Ret and Ednrb

Lignende værker

• A gene regulatory network explains RET–EDNRB epistasis in Hirschsprung disease
  af: Chatterjee, Sumantra, et al.
  Udgivet: (2019)
• Phenotype–genotype correlation in Hirschsprung disease is illuminated by comparative analysis of the RET protein sequence
  af: Kashuk, Carl S., et al.
  Udgivet: (2005)
• A human model for multigenic inheritance: Phenotypic expression in Hirschsprung disease requires both the RET gene and a new 9q31 locus
  af: Bolk, Stacey, et al.
  Udgivet: (2000)
• Double heterozygosity for a RET substitution interfering with splicing and an EDNRB missense mutation in Hirschsprung disease.
  af: Auricchio, A, et al.
  Udgivet: (1999)
• Population variation in total genetic risk of Hirschsprung disease from common RET, SEMA3 and NRG1 susceptibility polymorphisms
  af: Kapoor, Ashish, et al.
  Udgivet: (2015)