Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

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Targeted next-generation sequencing helps to decipher the genetic and phenotypic heterogeneity of hypertrophic cardiomyopathy Mitochondrial haplogroups in patients with rheumatoid arthritis: No association with disease and disease manifestations.

P2860

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P2860

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

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http://www.wikidata.org/entity/Q35552917

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2015 nî lūn-bûn

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2015年の論文

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2015年論文

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2015年論文

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2015年論文

@zh-hk

2015年論文

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2015年論文

@zh-tw

2015年论文

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name

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@ast

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@en

type

Item

label

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@ast

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@en

prefLabel

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@ast

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

@en

P1476

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy

@en

P2093

Christian M Hagen

http://www.w3.org/2001/XMLSchema#string

Frederik H Aidt

http://www.w3.org/2001/XMLSchema#string

Michael Christiansen

http://www.w3.org/2001/XMLSchema#string

Ole Havndrup

http://www.w3.org/2001/XMLSchema#string

Tam T Pham

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P2860

Mitochondrial haplogroups H and J: risk and protective factors for ischemic cardiomyopathy

The G x U wobble base pair. A fundamental building block of RNA structure crucial to RNA function in diverse biological systems

Reduced-median-network analysis of complete mitochondrial DNA coding-region sequences for the major African, Asian, and European haplogroups.

Clinical expression of Leber hereditary optic neuropathy is affected by the mitochondrial DNA-haplogroup background

Accurate energies of hydrogen bonded nucleic acid base pairs and triplets in tRNA tertiary interactions.

Mitochondrial tRNA mutations and disease

Strong purifying selection in transmission of mammalian mitochondrial DNA

A mitochondrial cytochrome b mutation but no mutations of nuclearly encoded subunits in ubiquinol cytochrome c reductase (complex III) deficiency

Mitochondrial DNA haplogroups in Spanish patients with hypertrophic cardiomyopathy

Diagnostic yield, interpretation, and clinical utility of mutation screening of sarcomere encoding genes in Danish hypertrophic cardiomyopathy patients and relatives

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e0124540

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scholarly article

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10.1371/JOURNAL.PONE.0124540

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English

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2015-04-29T00:00:00Z

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275660742

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25923817

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P921

mitochondrial DNA

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4414448

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Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

about

P2860

P2860

Private mitochondrial DNA variants in danish patients with hypertrophic cardiomyopathy.

description

name

type

label

prefLabel

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932

P356

P1433

P1476

P2093

P2860

P304

P31

P356

P407

P433

P478

P50

P577

P5875

P698

P921

P932