The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys–Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD)-Reference-Cited by-同舟云学术

The spectrum of FBN1, TGFβR1, TGFβR2 and ACTA2 variants in 594 individuals with suspected Marfan Syndrome, Loeys–Dietz Syndrome or Thoracic Aortic Aneurysms and Dissections (TAAD)

Published:2014-06 Issue:2 Volume:112 Page:171-176
ISSN:1096-7192
Container-title:Molecular Genetics and Metabolism
language:en
Short-container-title:Molecular Genetics and Metabolism

Author:

Lerner-Ellis Jordan P.,Aldubayan Saud H.,Hernandez Amy Lovelette,Kelly Melissa Allard,Stuenkel Aaron J.,Walsh Jennifer,Joshi Victoria A.

Publisher

Elsevier BV

Subject

Endocrinology,Genetics,Molecular Biology,Biochemistry,Endocrinology, Diabetes and Metabolism

Reference38 articles.

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5. Linkage of Marfan syndrome and a phenotypically related disorder to two different fibrillin genes;Lee;Nature,1991

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