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Nuclear-Mitochondrial Intergenomic Communication Disorders

dc.contributor.authorAlmeida, L.S.
dc.contributor.authorNogueira, C.
dc.contributor.authorVilarinho, L.
dc.date.accessioned2012-10-24T16:44:36Z
dc.date.available2012-10-24T16:44:36Z
dc.date.issued2012
dc.description.abstractThe focus of this chapter is to review the clinical and molecular etiologies of nuclear defects involved in mtDNA stability and in mitochondrial protein synthesis. The overview done here will hopefully provide insights towards best diagnostic strategies of mitochondrial cross–talk disorders, being useful for clinicians when facing similar cases. Additionally we will present a diagnostic algorithm for these diseases based on our knowledge.por
dc.identifier.citationIn Skeletal Muscle- From Myogenesis to Clinical Relations. 2012: 293-316por
dc.identifier.isbn978-953-51-0712-5
dc.identifier.urihttp://hdl.handle.net/10400.18/1055
dc.language.isoengpor
dc.peerreviewedyespor
dc.publisherInTechpor
dc.relation.publisherversionhttp://www.intechopen.com/books/skeletal-muscle-from-myogenesis-to-clinical-relations/nuclear-mitochondrial-intergenomic-communication-disorderspor
dc.subjectIntergenomic Communication disorderspor
dc.subjectmtDNApor
dc.subjectDoenças Genéticaspor
dc.titleNuclear-Mitochondrial Intergenomic Communication Disorderspor
dc.typebook part
dspace.entity.typePublication
oaire.citation.endPage316por
oaire.citation.startPage293por
rcaap.rightsopenAccesspor
rcaap.typebookPartpor

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