ScholarLens Back to search
2014•Molecular Genetics and MetabolismRequires access

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)

Jordan P. Lerner‐Ellis, Saud H. AlDubayan, Amy Hernandez, Melissa Kelly, Aaron J. Stuenkel, Jennifer Walsh, Victoria A. Joshi

Open publisher page 62 citations

Abstract

This record does not include an abstract. Use the full-text link above if available.

About this research paper

What this paper is about

An abstract is not available in the OpenAlex record for this paper.

Why it matters

OpenAlex reports 62 citations for this work. Citation counts describe recorded attention and do not establish research quality.

Key contribution

A contribution statement is not available in the OpenAlex record.

Method / approach

Method details are not available in the OpenAlex metadata.

Main findings

Findings are not separately available in the OpenAlex metadata.

Limitations

Limitations are not available in the OpenAlex metadata.

Applications

Application details are not available in the OpenAlex metadata.

Key concepts: Marfan syndrome, Medicine, Transforming growth factor, Thoracic aortic aneurysm, Aortic aneurysm, Internal medicine, Aorta

Related papers

Related paper 1Related paper 2
Back to paper searchBrowse research topicsOriginal source
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) — Research Paper | ScholarLens