Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy. (Q46246554)

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23 February 2020

title

Mitochondrial tRNA glutamine variant in hypertrophic cardiomyopathy (English)

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23 February 2020

author

Sinda Zarrouk Mahjoub

1

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23 February 2020

author name string

S Mehri

2

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23 February 2020

F Ouarda

3

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23 February 2020

J Finsterer

4

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23 February 2020

R Boussaada

5

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23 February 2020

publication date

27 September 2013

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23 February 2020

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23 February 2020

volume

40

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23 February 2020

issue

3

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23 February 2020

page(s)

436-441

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Mitochondrial tRNA 3' end metabolism and human disease.

23 February 2020

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Genetic variants in mitochondrial tRNA genes are associated with essential hypertension in a Chinese Han population

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A surviving case of mitochondrial cardiomyopathy diagnosed from the symptoms of multiple organ dysfunction syndrome

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The mitochondrial DNA mutation T12297C affects a highly conserved nucleotide of tRNA(Leu(CUN)) and is associated with dilated cardiomyopathy

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A heteroplasmic mitochondrial DNA 3310 mutation in the ND1 gene in a patient with type 2 diabetes, hypertrophic cardiomyopathy, and mental retardation

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12 December 2020

Exhaustive Scanning Approach to Screen All the Mitochondrial tRNA Genes for Mutations and Its Application to the Investigation of 35 Independent Patients with Mitochondrial Disorders

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12 December 2020

Phenotypic spectrum and patterns of left ventricular hypertrophy in hypertrophic cardiomyopathy: Morphologic observations and significance as assessed by two-dimensional echocardiography in 600 patients

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Fatal hypertrophic cardiomyopathy associated with an A8296G mutation in the mitochondrial tRNA(Lys) gene

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A novel mitochondrial DNA tRNAIle (m.4322dupC) mutation associated with idiopathic dilated cardiomyopathy

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Identifiers

DOI

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23 February 2020

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