Association of G71R Mutation of the UGT1A1 Gen with Neonatal Hyper Bilirubinemia in the Iranian Population

Association of G71R Mutation of the UGT1A1 Gen with Neonatal Hyper Bilirubinemia in the Iranian Population

Objective: Jaundice with indirect hyperbilirubinemia is one of the most common neonatal problems that occur in 60% of term and 80% of preterm neonates but the causes are mostly unknown. It is suggested that race plays an important role in the prevalence of hyperbilirubinemia. It is a common problem...

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Dettagli Bibliografici
Autori principali:	Ebrahim Dastgerdy, Gholamali Mamori, Jalil Afshari, Reza Saeedi, Fatemeh Shahbazi, Mahboobeh Shirazi
Natura:	Articolo
Lingua:	English
Pubblicazione:	Tehran University of Medical Sciences 2012-03-01
Serie:	Journal of Family and Reproductive Health
Soggetti:	Hyperbilirubinemia Newborn UGT1A1 gene Iran polymorphism
Accesso online:	https://jfrh.tums.ac.ir/index.php/jfrh/article/view/140

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