The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype.

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P1476

The m.7510T>C mutation: Hearing impairment and a complex neurologic phenotype

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P2093

Kari Majamaa

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Maria Gardberg

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P2860

Ancient voyaging and Polynesian origins

Naturally occurring mutations in human mitochondrial pre-tRNASer(UCN) can affect the transfer ribonuclease Z cleavage site, processing kinetics, and substrate secondary structure

Atypical muscle pathology and a survey of cis-mutations in deaf patients harboring a 1555 A-to-G point mutation in the mitochondrial ribosomal RNA gene

Updated comprehensive phylogenetic tree of global human mitochondrial DNA variation

A novel point mutation in the mitochondrial tRNA(Ser(UCN)) gene detected in a family with MERRF/MELAS overlap syndrome

Non-syndromic Hearing Impairment in a Hungarian Family with the m.7510T>C Mutation of Mitochondrial tRNA(Ser(UCN)) and Review of Published Cases.

Maternally inherited non-syndromic hearing impairment in a Spanish family with the 7510T>C mutation in the mitochondrial tRNA(Ser(UCN)) gene.

Cerebellar ataxia in patients with mitochondrial DNA disease: a molecular clinicopathological study.

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

A novel mutation in the mitochondrial tRNA(Ser(UCN)) gene in a family with non-syndromic sensorineural hearing impairment.

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e00859

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scholarly article

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10.1002/BRB3.859

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P433

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P478

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P50

Mika H Martikainen

Laura Kytövuori

P577

2017-11-19T00:00:00Z

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P698

29299381

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P932

5745241

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