Publication:
A rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emirates

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dc.contributor.authorAbou Tayoun, Ahmad N.
dc.contributor.authorAlsheikh-Ali, Alawi
dc.date.accessioned2023-12-18T07:50:41Z
dc.date.available2023-12-18T07:50:41Z
dc.date.issued2023
dc.description.abstractIntroduction: A large body of evidence now supports use of rapid whole-genome sequencing (rWGS) as a cost-effective tool for timely diagnosis and tailored management of critically ill children with rare diseases. However, efficacy has so far been demonstrated only in high-income settings, which has led to disparate implementation of and variable access to rWGS.en_US
dc.identifier.other204-2023.159
dc.identifier.urihttps://repository.mbru.ac.ae/handle/1/1415
dc.language.isoenen_US
dc.subjectWhole-Genome Sequencingen_US
dc.subjectWhole-Genome Sequencing Serviceen_US
dc.subjectRare Diseasesen_US
dc.subjectInfantsen_US
dc.subjectUnited Arab Emiratesen_US
dc.titleA rapid whole-genome sequencing service for infants with rare diseases in the United Arab Emiratesen_US
dc.typeArticleen_US
dspace.entity.typePublicationen_US

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