A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy
Crossref DOI link: https://0-doi-org.brum.beds.ac.uk/10.1186/s12881-016-0267-5
Published Online: 2016-01-14
Published Print: 2016-12
Update policy: https://0-doi-org.brum.beds.ac.uk/10.1007/springer_crossmark_policy
Al-Hassnan, Zuhair N.
Shinwari, Zarghuna MA.
Wakil, Salma M.
Tulbah, Sahar
Mohammed, Shamayel
Rahbeeni, Zuhair
Alghamdi, Mohammed
Rababh, Monther
Colak, Dilek
Kaya, Namik
Al-Fayyadh, Majid
Alburaiki, Jehad
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