MtDNA-related idiopathic dilated cardiomyopathy.

作者信息

Tessa A, Vilarinho L, Casali C, Santorelli F M

出版信息

Eur J Hum Genet. 1999 Dec;7(8):847-8. doi: 10.1038/sj.ejhg.5200380.

DOI:10.1038/sj.ejhg.5200380

PMID:10602359

Abstract

摘要

相似文献

Eur J Hum Genet. 1999 Dec;7(8):847-8. doi: 10.1038/sj.ejhg.5200380.

Maternally inherited cardiomyopathy: a new phenotype associated with the A to G AT nt.3243 of mitochondrial DNA (MELAS mutation).

Muscle Nerve. 1997 Feb;20(2):221-5. doi: 10.1002/(sici)1097-4598(199702)20:2<221::aid-mus13>3.0.co;2-5.

Mitochondrial DNA in idiopathic cardiomyopathy.

Eur Heart J. 1998 Nov;19(11):1725-9. doi: 10.1053/euhj.1998.1125.

Mitochondrial cardiomyopathies: how to identify candidate pathogenic mutations by mitochondrial DNA sequencing, MITOMASTER and phylogeny.

Eur J Hum Genet. 2011 Feb;19(2):200-7. doi: 10.1038/ejhg.2010.169. Epub 2010 Oct 27.

The mitochondrial DNA C3303T mutation can cause cardiomyopathy and/or skeletal myopathy.

J Pediatr. 1999 Aug;135(2 Pt 1):197-202. doi: 10.1016/s0022-3476(99)70022-3.

A new mtDNA mutation in the tRNA(Leu(UUR)) gene associated with maternally inherited cardiomyopathy.

Hum Mutat. 1994;3(1):37-43. doi: 10.1002/humu.1380030107.

Cardiovascular Involvement in mtDNA Disease: Diagnosis, Management, and Therapeutic Options.

Heart Fail Clin. 2022 Jan;18(1):51-60. doi: 10.1016/j.hfc.2021.07.003. Epub 2021 Oct 26.

The mitochondrial A3243G mutation presenting as severe cardiomyopathy.

J Med Genet. 1997 Jul;34(7):607-9. doi: 10.1136/jmg.34.7.607.

Patients with idiopathic cardiomyopathy belong to the same mitochondrial DNA gene family of Parkinson's disease and mitochondrial encephalomyopathy.

Biochem Biophys Res Commun. 1991 May 31;177(1):518-25. doi: 10.1016/0006-291x(91)92014-b.

Maternally inherited cardiomyopathy: an atypical presentation of the mtDNA 12S rRNA gene A1555G mutation.

Am J Hum Genet. 1999 Jan;64(1):295-300. doi: 10.1086/302188.

引用本文的文献

Mitochondrial Cardiomyopathy: The Roles of mt-tRNA Mutations.

J Clin Med. 2022 Oct 30;11(21):6431. doi: 10.3390/jcm11216431.

Frequency of mitochondrial transfer RNA mutations and deletions in 225 patients presenting with respiratory chain deficiencies.

J Med Genet. 2001 Oct;38(10):665-73. doi: 10.1136/jmg.38.10.665.

文献AI研究员

20分钟写一篇综述，助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型，支持多种主流文档格式。

立即体验