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dc.contributor.authorWilliams, JLen_US
dc.contributor.authorSmith, CJen_US
dc.contributor.authorMastroianni, Gen_US
dc.contributor.authorStewart, Men_US
dc.contributor.authorCutillas, Pen_US
dc.contributor.authorTinker, Aen_US
dc.contributor.authorMetherell, Len_US
dc.date.accessioned2024-04-29T09:47:55Z
dc.date.issued2023-08-04en_US
dc.identifier.issn0009-7330en_US
dc.identifier.urihttps://qmro.qmul.ac.uk/xmlui/handle/123456789/96506
dc.publisherWolters Kluweren_US
dc.relation.ispartofCirculation Researchen_US
dc.subjectCardiovascularen_US
dc.subjectGeneticsen_US
dc.subjectHeart Diseaseen_US
dc.subjectRare Diseasesen_US
dc.subject2 Aetiologyen_US
dc.subject2.1 Biological and endogenous factorsen_US
dc.subjectCardiovascularen_US
dc.titleAbstract P2043: Loss Of Full-length Mylk3 Causes Dilated Cardiomyopathy Via A Myl2-independent Mechanismen_US
dc.typeArticle
dc.identifier.doi10.1161/res.133.suppl_1.p2043en_US
pubs.issueSuppl_1en_US
pubs.notesNot knownen_US
pubs.volume133en_US
rioxxterms.funderDefault funderen_US
rioxxterms.identifier.projectDefault projecten_US
qmul.funderThe role of MYLK3 in cardiac signalling and development::British Heart Foundationen_US
qmul.funderThe role of MYLK3 in cardiac signalling and development::British Heart Foundationen_US


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