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Mutation analysis of the PAH gene in phenylketonuria patients from Rio de Janeiro, Southeast Brazil.

Eduardo Vieira NetoFrancisco LaranjeiraDulce QuelhasIsaura RibeiroAlexandre SeabraNicole MineiroLilian D M CarvalhoLúcia LacerdaMárcia G Ribeiro
Published in: Molecular genetics & genomic medicine (2018)
The three most frequent pathogenic variants in our study (34.8% of the alleles) were also the most common in other Brazilian states, Portugal, and Spain (p.V388M, p.R261Q, IVS10-11G>A), corroborating that the Iberian Peninsula is the major source of PAH mutations in Rio de Janeiro. Pathogenic variants that have other geographical origins, such IVS2+5G>C, p.G352Vfs*48, and IVS12+1G>A were also detected. Genetic drift and founder effect may have also played a role in the mutation spectrum we observed.
Keyphrases
  • copy number
  • end stage renal disease
  • genome wide
  • ejection fraction
  • newly diagnosed
  • chronic kidney disease
  • prognostic factors