Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. (Q52652833)
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scientific article published on 13 August 2014
| Language | Label | Description | Also known as |
|---|---|---|---|
| English | Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. |
scientific article published on 13 August 2014 |
Statements
Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness. (English)
Iftikhar J Kullo
Khader Shameer
Eric W Klee
Angela K Dalenberg
13 August 2014
7
5
607-614