New cardiac and skeletal protein aggregate myopathy associated with combined MuRF1 and MuRF3 mutations: [Human Molecular Genetics, 24, 13, (2015) 3638-3650] DOI: 10.1093/hmg/ddv108 [Erratum]Show others and affiliations
2015 (English)In: Human Molecular Genetics, ISSN 0964-6906, E-ISSN 1460-2083, Vol. 24, no 21, p. 6264-6264Article in journal (Refereed) Published
Place, publisher, year, edition, pages
Oxford University Press, 2015. Vol. 24, no 21, p. 6264-6264
National Category
Neurology
Research subject
Medical sciences
Identifiers
URN: urn:nbn:se:his:diva-11987DOI: 10.1093/hmg/ddv311ISI: 000363024000025PubMedID: 26345447Scopus ID: 2-s2.0-84949188726OAI: oai:DiVA.org:his-11987DiVA, id: diva2:907145
2016-02-262016-02-262017-11-30Bibliographically approved