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dc.contributor.authorSoria-Valles, C.en
dc.contributor.authorCarrero, D.en
dc.contributor.authorGabau, E.en
dc.contributor.authorVelasco, G.en
dc.contributor.authorQuesada, V.en
dc.contributor.authorBárcena, C.en
dc.contributor.authorMoens, M.en
dc.contributor.authorFieggen, K.en
dc.contributor.authorMöhrcken, S.en
dc.contributor.authorOwens, Martinaen
dc.contributor.authorPuente, D. A.en
dc.contributor.authorAsensio, Ó.en
dc.contributor.authorLoeys, B.en
dc.contributor.authorPérez, A.en
dc.contributor.authorBenoit, V.en
dc.contributor.authorWuyts, W.en
dc.contributor.authorLévy, N.en
dc.contributor.authorHennekam, R. C.en
dc.contributor.authorDe Sandre-Giovannoli, A.en
dc.contributor.authorLópez-Otín, C.en
dc.identifier.citationNovel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation. 2016: J. Med. Genet.en
dc.description.abstractProgeroid syndromes are genetic disorders that recapitulate some phenotypes of physiological ageing. Classical progerias, such as Hutchinson-Gilford progeria syndrome (HGPS), are generally caused by mutations in LMNA leading to accumulation of the toxic protein progerin and consequently, to nuclear envelope alterations. In this work, we describe a novel phenotypic feature of the progeria spectrum affecting three unrelated newborns and identify its genetic cause.en
dc.rightsArchived with thanks to Journal of Medical Geneticsen
dc.subjectWessex Classification Subject Headings::Oncology. Pathology.::Geneticsen
dc.titleNovel LMNA mutations cause an aggressive atypical neonatal progeria without progerin accumulation.en
dc.typeJournal Articleen
dc.identifier.journalJournal of medical geneticsen
dc.type.versionIn press (epub ahead of print)en
dc.description.admin-noteAccepted manuscript, no embargo.en

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