标题
MT-CYBmutations in hypertrophic cardiomyopathy
作者
关键词
-
出版物
Molecular Genetics & Genomic Medicine
Volume 1, Issue 1, Pages 54-65
出版商
Wiley
发表日期
2013-04-12
DOI
10.1002/mgg3.5
参考文献
相关参考文献
注意:仅列出部分参考文献,下载原文获取全部文献信息。- Mitochondrial DNA variant associated with Leber hereditary optic neuropathy and high-altitude Tibetans
- (2012) F. Ji et al. PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA
- Investigating diproline segments in proteins: Occurrences, conformation and classification
- (2011) Indranil Saha et al. BIOPOLYMERS
- Investigation of mitochondrial sequence variants associated with aminoglycoside-induced ototoxicity in South African TB patients on aminoglycosides
- (2010) Hanniqué Human et al. BIOCHEMICAL AND BIOPHYSICAL RESEARCH COMMUNICATIONS
- Mitochondria in heart failure
- (2010) M. G. Rosca et al. CARDIOVASCULAR RESEARCH
- Malignant and benign mutations in familial cardiomyopathies: Insights into mutations linked to complex cardiovascular phenotypes
- (2010) Qian Xu et al. JOURNAL OF MOLECULAR AND CELLULAR CARDIOLOGY
- Maternally inherited hearing loss is associated with the novel mitochondrial tRNASer(UCN) 7505T>C mutation in a Han Chinese family
- (2010) Xiaowen Tang et al. MOLECULAR GENETICS AND METABOLISM
- I-TASSER: a unified platform for automated protein structure and function prediction
- (2010) Ambrish Roy et al. Nature Protocols
- From protons to OXPHOS supercomplexes and Alzheimer's disease: Structure–dynamics–function relationships of energy-transducing membranes
- (2009) H. Seelert et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mitochondrial DNA mutations and human disease
- (2009) Helen A.L. Tuppen et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- The Dawn of Human Matrilineal Diversity
- (2008) Doron M. Behar et al. AMERICAN JOURNAL OF HUMAN GENETICS
- Pathogenic Mitochondrial DNA Mutations Are Common in the General Population
- (2008) Hannah R. Elliott et al. AMERICAN JOURNAL OF HUMAN GENETICS
- 20 years of human mtDNA pathologic point mutations: Carefully reading the pathogenicity criteria
- (2008) Julio Montoya et al. BIOCHIMICA ET BIOPHYSICA ACTA-BIOENERGETICS
- Mitochondrial oxidative stress and dysfunction in myocardial remodelling
- (2008) H. Tsutsui et al. CARDIOVASCULAR RESEARCH
- Age- and gender-specific mortality rates in childhood hypertrophic cardiomyopathy
- (2008) I. Ostman-Smith et al. EUROPEAN HEART JOURNAL
- Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives
- (2008) Paal Skytt Andersen et al. HUMAN MUTATION
- Progressive Encephalopathy and Complex I Deficiency Associated with Mutations in MTND1
- (2008) A.-R. Moslemi et al. NEUROPEDIATRICS
- Detection of unrecognized low-level mtDNA heteroplasmy may explain the variable phenotypic expressivity of apparently homoplasmic mtDNA mutations
- (2007) Ester Ballana et al. HUMAN MUTATION
Find Funding. Review Successful Grants.
Explore over 25,000 new funding opportunities and over 6,000,000 successful grants.
ExploreBecome a Peeref-certified reviewer
The Peeref Institute provides free reviewer training that teaches the core competencies of the academic peer review process.
Get Started