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Paper Details

Whole exome sequencing for the identification of a new mutation in TGFB2 involved in a familial case of non-syndromic aortic disease.
Clin Chim Acta
15
2014
Author NameAffiliation
Irene ValenzuelaHospital Universitari Vall d'Hebron
Angel CarracedoKing Abdulaziz University
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Release 1.2