Missense Mutations and Gene Interruption inPROSIT240, a NovelTRAP240-Like Gene, in Patients With Congenital Heart Defect (Transposition of the Great Arteries)-Reference-Cited by-同舟云学术

Missense Mutations and Gene Interruption inPROSIT240, a NovelTRAP240-Like Gene, in Patients With Congenital Heart Defect (Transposition of the Great Arteries)

Published:2003-12-09 Issue:23 Volume:108 Page:2843-2850
ISSN:0009-7322
Container-title:Circulation
language:en
Short-container-title:Circulation

Author:

Muncke Nadja¹,Jung Christine¹,Rüdiger Heinz¹,Ulmer Herbert¹,Roeth Ralph¹,Hubert Annette¹,Goldmuntz Elizabeth¹,Driscoll Deborah¹,Goodship Judith¹,Schön Karin¹,Rappold Gudrun¹

Affiliation:

1. From the Institut für Humangenetik (N.M., C.G., R.R., A.H., K.S., G.R.), Universität Heidelberg, and the Abteilung für Kardiologie (H.R., H.U.), Kinderklinik Heidelberg, Heidelberg, Germany; the Division of Cardiology (E.G., D.D.), Department of Pediatrics, University of Pennsylvania School of Medicine, Philadelphia, Pa; and the Institute of Human Genetics (J.G.), International Center for Life, Newcastle upon Tyne, Great Britain.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Physiology (medical),Cardiology and Cardiovascular Medicine

Reference36 articles.

1. Incidence of congenital heart disease: I. Postnatal incidence

2. Incidence of congenital heart disease: I. Postnatal incidence

3. Kardiovaskuläre Fehlbildungen in Bayern 19841991 (Cardiovascular malformations in Bavaria, Germany, 19841991)

4. Congenital heart malformations: prevalence, severity, survival, and quality of life

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