(Q44475588)

3 December 2017

title

Increased variation in mtDNA in patients with familial sensorineural hearing impairment (English)

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3 December 2017

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Jukka S Moilanen

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author name string

Mervi S Lehtonen

series ordinal

1

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3 December 2017

Kari Majamaa

series ordinal

3

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3 December 2017

publication date

12 June 2003

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3 December 2017

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3 December 2017

volume

113

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3 December 2017

issue

3

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3 December 2017

page(s)

220-227

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A General Model for the Genetic Analysis of Pedigree Data

3 December 2017

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Hearing impairment in patients with 3243A-->G mtDNA mutation: phenotype and rate of progression.

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12 December 2020

Frequency of mitochondrial DNA point mutations among patients with familial sensorineural hearing impairment.

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12 December 2020

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Haplotype and phylogenetic analyses suggest that one European-specific mtDNA background plays a role in the expression of Leber hereditary optic neuropathy by increasing the penetrance of the primary mutations 11778 and 14484.

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Maternally inherited hearing loss in a large kindred with a novel T7511C mutation in the mitochondrial DNA tRNA(Ser(UCN)) gene

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Epidemiology of A3243G, the mutation for mitochondrial encephalomyopathy, lactic acidosis, and strokelike episodes: prevalence of the mutation in an adult population.

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Myoclonic epilepsy and ragged-red fiber disease (MERRF) is associated with a mitochondrial DNA tRNA(Lys) mutation

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Compilation of tRNA sequences and sequences of tRNA genes

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mtDNA haplotype analysis in Finnish families with leber hereditary optic neuroretinopathy

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Hearing impairment and neurological dysfunction associated with a mutation in the mitochondrial tRNASer(UCN) gene.

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Mitochondrial ribosomal RNA mutation associated with both antibiotic-induced and non-syndromic deafness

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10.1007/S00439-003-0966-9

Identifiers

DOI

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3 December 2017

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