UGT1A1 gene linkage analysis: application of polymorphic markers rs4148326/rs4124874 in the Iranian population

OBJECTIVE(S): Mutations in the UGT1A1 gene are responsible for hyperbilirubinemia syndromes including Crigler-Najjar type 1 and 2 and Gilbert syndrome. In view of the genetic heterogeneity and involvement of large numbers of the disease causing mutations, the application of polymorphic markers in th...

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Detalles Bibliográficos
Autores principales: Nadeali, Zakiye, Vallian, Sadeq
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Mashhad University of Medical Sciences 2017
Materias:
Original Article
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651473/
https://www.ncbi.nlm.nih.gov/pubmed/29085579
http://dx.doi.org/10.22038/IJBMS.2017.9109

Internet

https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5651473/
https://www.ncbi.nlm.nih.gov/pubmed/29085579
http://dx.doi.org/10.22038/IJBMS.2017.9109

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