DOI:
10.1055/s-00029027
Journal of Pediatric Genetics
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References
Shameer K, Klee EW, Dalenberg AK, Kullo IJ.
Whole exome sequencing implicates an INO80D mutation in a syndrome of aortic hypoplasia, premature atherosclerosis, and arterial stiffness.
Circ Cardiovasc Genet 2014;
7 (05) 607-614
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