Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy-Reference-Cited by-同舟云学术

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Cardiac mitochondrial dysfunction and DNA depletion in children with hypertrophic cardiomyopathy

Published:1997-09 Issue:5 Volume:20 Page:674-680
ISSN:0141-8955
Container-title:Journal of Inherited Metabolic Disease
language:en
Short-container-title:J Inherit Metab Dis

Author:

Marin-Garcia J.¹²,Ananthakrishnan R.¹,Goldenthal M. J.¹,Filiano J. J.³,Perez-Atayde A.⁴

Affiliation:

1. The Molecular Cardiology Institute; Highland Park New Jersey

2. ; St. Barnabas Medical Center; Livingston New Jersey USA

3. ; Department of Pediatrics; Dartmouth Hitchcock Medical Center; Lebanon New Hampshire USA

4. ; Children's Hospital; Harvard Medical School; Boston Massachusetts USA

Publisher

Wiley

Subject

Genetics (clinical),Genetics

Link

http://onlinelibrary.wiley.com/wol1/doi/10.1023/A:1005322409330/fullpdf

Reference23 articles.

1. Prognostic implications of novel β cardiac myosin heavy chain gene mutations that cause familial hypertrophic cardiomyopathy;Anan;J Clin Invest,1994

2. Depletion of mitochondrial deoxyribonucleic acid in a family with fatal neonatal liver disease;Bakker;J Pediatr,1996

3. A novel mtDNA point mutation in maternally inherited cardiomyopathy;Casali;Biochem Biophys Res Commun,1995

4. Dilated cardiomyopathy in a zidovudine treated AIDS patient;D'Amati;Cardiovasc Pathol,1992

5. Cardiomyopathy associated with antiretroviral therapy in patients with HIV infection: a report of 6 cases;Herskowitz;Ann Intern Med,1992

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