Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension-Reference-Cited by-同舟云学术

Investigation of Second Genetic Hits at the BMPR2 Locus as a Modulator of Disease Progression in Familial Pulmonary Arterial Hypertension

Published:2005-02-08 Issue:5 Volume:111 Page:607-613
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Machado Rajiv D.¹,James Victoria¹,Southwood Mark¹,Harrison Rachel E.¹,Atkinson Carl¹,Stewart Susan¹,Morrell Nicholas W.¹,Trembath Richard C.¹,Aldred Micheala A.¹

Affiliation:

1. From the Division of Medical Genetics (R.D.M., V.J., R.E.H., R.C.T., M.A.A.), Departments of Genetics and Cardiovascular Sciences, University of Leicester, Leicester, UK; and the Division of Respiratory Medicine (M.S., C.A., S.S., N.W.M.), Department of Medicine, University of Cambridge School of Clinical Medicine, Addenbrookes and Papworth Hospitals, Cambridge, UK.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference26 articles.

1. Primary Pulmonary Hypertension

2. Primary pulmonary hypertension

3. Primary Pulmonary Hypertension

4. Heterozygous germline mutations in BMPR2, encoding a TGF-β receptor, cause familial primary pulmonary hypertension

5. Familial Primary Pulmonary Hypertension (Gene PPH1) Is Caused by Mutations in the Bone Morphogenetic Protein Receptor–II Gene

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