✦ LIBER ✦

Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure

✍ Scribed by Olson, T. M.

Book ID: 121159429
Publisher: American Association for the Advancement of Science
Year: 1998
Tongue: English
Weight: 359 KB
Volume: 280
Category: Article
ISSN: 0036-8075
DOI: 10.1126/science.280.5364.750

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Dilated Cardiomyopathy and Heart Failure

Dilated Cardiomyopathy and Heart Failure Caused by a Mutation in Phospholamban

✍ Schmitt, J. P. 📂 Article 📅 2003 🏛 American Association for the Advancement of Scienc 🌐 English ⚖ 501 KB

Epidemiology of cardiac actin gene mutat

Epidemiology of cardiac actin gene mutations in dilated cardiomyopathy

✍ Ronald Zolty; Gary L. Brodsky; M. Benjamin Perryman; Michael R. Bristow; Luisa M 📂 Article 📅 1999 🏛 Elsevier Science 🌐 English ⚖ 130 KB

Molecular epidemiology of cardiac actin

Molecular epidemiology of cardiac actin gene mutations in dilated cardiomyopathy

✍ Ronald Zolty; G. Passarino; M.R. Taylor; A. Moss; L. Mestroni; M.R. Bristow 📂 Article 📅 2002 🏛 Elsevier Science 🌐 English ⚖ 153 KB

Dilated Cardiomyopathies as a Cause of C

Dilated Cardiomyopathies as a Cause of Congestive Heart Failure

✍ Bernhard Maisch; Arsen D. Ristić; Günter Hufnagel; Reinhard Funck; Peter Alter; 📂 Article 📅 2002 🏛 Urban and Vogel 🌐 German ⚖ 425 KB

Hypothyroid Cardiomyopathy: A Reversible

Hypothyroid Cardiomyopathy: A Reversible Form of Systolic Heart Failure

✍ Ajay J. Kirtane; Warren J. Manning 📂 Article 📅 2011 🏛 Elsevier Science 🌐 English ⚖ 306 KB

Mutational analysis of the cardiac actin

Mutational analysis of the cardiac actin gene in familial and sporadic dilated cardiomyopathy

✍ Takai, Eiji; Akita, Hozuka; Shiga, Nobuyuki; Kanazawa, Kenji; Yamada, Shinichiro 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 14 KB 👁 2 views

Dilated cardiomyopathy (DCM) results in part from genetic disorders. Recently, missense mutations of the cardiac actin gene have been reported to cause DCM. We studied 136 Japanese DCM cases to elucidate how frequently the gene mutations are involved in its pathogenesis. Genomic DNA samples were obt