A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy (Q28116355)
Jump to navigation
Jump to search
scientific journal article
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy |
scientific journal article |
Statements
2 references
A substitution mutation in cardiac ubiquitin ligase, FBXO32, is associated with an autosomal recessive form of dilated cardiomyopathy (English)
2 references
Sahar Tulbah
2 references
Shamayel Mohammed
2 references
Zuhair Rahbeeni
2 references
Mohammed Alghamdi
2 references
Monther Rababh
2 references
Namik Kaya
2 references
Majid Al-Fayyadh
2 references
Jehad Alburaiki
2 references
Zuhair N Al-Hassnan
Zarghuna Ma Shinwari
14 January 2016
2 references
2 references
17
2 references
3
2 references
Identifiers
2 references