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PCR in the Analysis of Clinical Samples: Prenatal and Postnatal Diagnosis of Inborn Errors of Metabolism

dc.contributor.authorVilarinho, Laura
dc.contributor.authorNogueira, Célia
dc.date.accessioned2018-02-19T17:07:32Z
dc.date.available2018-02-19T17:07:32Z
dc.date.issued2017-05-25
dc.description.abstractInborn errors of metabolism (IEMs) are individually rare but collectively common. As more and more enes are cloned and specific disease-causing mutations are identified, the diagnosis of IEMs is becoming increasingly confirmed by mutation analysis. Diagnosis is important not only for treatment and prognosis but also for genetic counselling and prenatal diagnosis in subsequent pregnancies. A wide range of molecular methods is available for the identification of mutations and other DNA variants, most of which are based on the Polymerase Chain Reaction (PCR). In this chapter, we focus on PCR-based methods for the detection of point mutations or small deletions/insertions as these are the most frequent causes of IEMs.pt_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.identifier.citationMethods Mol Biol. 2017;1620:213-224. doi: 10.1007/978-1-4939-7060-5_15.pt_PT
dc.identifier.doi10.1007/978-1-4939-7060-5_15pt_PT
dc.identifier.isbn978-1-4939-7059-9
dc.identifier.urihttp://hdl.handle.net/10400.18/4974
dc.language.isoengpt_PT
dc.peerreviewedyespt_PT
dc.publisherSpringer Science and Business Mediapt_PT
dc.relation.publisherversionhttps://link.springer.com/protocol/10.1007%2F978-1-4939-7060-5_15pt_PT
dc.subjectPCRpt_PT
dc.subjectIEMpt_PT
dc.subjectPrenatal Molecular Diagnosispt_PT
dc.subjectPostnatal Molecular Diagnosispt_PT
dc.subjectDoenças Genéticaspt_PT
dc.titlePCR in the Analysis of Clinical Samples: Prenatal and Postnatal Diagnosis of Inborn Errors of Metabolismpt_PT
dc.typebook part
dspace.entity.typePublication
oaire.citation.endPage224pt_PT
oaire.citation.startPage213pt_PT
oaire.citation.titleMethods in Molecular Biologypt_PT
rcaap.rightsrestrictedAccesspt_PT
rcaap.typebookPartpt_PT

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