Literature DB >> 9339712

A novel mitochondrial tRNA isoleucine gene mutation causing chronic progressive external ophthalmoplegia.

P F Chinnery1, M A Johnson, R W Taylor, W F Durward, D M Turnbull.   

Abstract

We report a sporadic case of chronic progressive external ophthalmoplegia that developed during childhood and was associated with ragged-red and cytochrome c oxidase (COX)-negative fibers in skeletal muscle. Sequencing of all the mitochondrial transfer RNA (tRNA) genes identified a single potentially pathogenic mutation--a T to C transition at position 4274 in the tRNA(Ile) gene. This mutation was not present in skeletal muscle from 79 controls, and the level of the mutation in COX-negative fibers was significantly greater than the level in COX-positive fibers.

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Year:  1997        PMID: 9339712     DOI: 10.1212/wnl.49.4.1166

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  9 in total

Review 1.  Mitochondrial DNA analysis: polymorphisms and pathogenicity.

Authors:  P F Chinnery; N Howell; R M Andrews; D M Turnbull
Journal:  J Med Genet       Date:  1999-07       Impact factor: 6.318

Review 2.  Clinical mitochondrial genetics.

Authors:  P F Chinnery; N Howell; R M Andrews; D M Turnbull
Journal:  J Med Genet       Date:  1999-06       Impact factor: 6.318

3.  A novel mutation in the tRNAIle gene (MTTI) affecting the variable loop in a patient with chronic progressive external ophthalmoplegia (CPEO).

Authors:  Andres Berardo; Jorida Coku; Bulent Kurt; Salvatore DiMauro; Michio Hirano
Journal:  Neuromuscul Disord       Date:  2010-02-10       Impact factor: 4.296

4.  Impairment of mitochondrial tRNAIle processing by a novel mutation associated with chronic progressive external ophthalmoplegia.

Authors:  A Schaller; R Desetty; D Hahn; C B Jackson; J-M Nuoffer; S Gallati; L Levinger
Journal:  Mitochondrion       Date:  2011-02-01       Impact factor: 4.160

5.  Recurrent myoglobinuria in a sporadic patient with a novel mitochondrial DNA tRNA(Ile) mutation.

Authors:  Valentina Emmanuele; Evangelia Sotiriou; Maryam Shirazi; Kurenai Tanji; Ronald G Haller; Katja Heinicke; Peter E Bosch; Michio Hirano; Salvatore DiMauro
Journal:  J Neurol Sci       Date:  2011-02-15       Impact factor: 3.181

6.  A novel mitochondrial tRNA(Val) T1658C mutation identified in a CPEO family.

Authors:  Naihong Yan; Shuping Cai; Bo Guo; Yi Mou; Jing Zhu; Jun Chen; Ting Zhang; Ronghua Li; Xuyang Liu
Journal:  Mol Vis       Date:  2010-08-25       Impact factor: 2.367

7.  Mitochondrial DNA abnormalities in ophthalmological disease.

Authors:  Grainne S Gorman; Robert W Taylor
Journal:  Saudi J Ophthalmol       Date:  2011-02-18

8.  A novel mitochondrial tRNA(Ala) gene variant causes chronic progressive external ophthalmoplegia in a patient with Huntington disease.

Authors:  Massimiliano Filosto; Gaetana Lanzi; Claudia Nesti; Valentina Vielmi; Eleonora Marchina; Anna Galvagni; Silvia Giliani; Filippo M Santorelli; Alessandro Padovani
Journal:  Mol Genet Metab Rep       Date:  2016-02-27

9.  Disclosing the functional changes of two genetic alterations in a patient with Chronic Progressive External Ophthalmoplegia: Report of the novel mtDNA m.7486G>A variant.

Authors:  Mafalda Bacalhau; Marta Simões; Mariana C Rocha; Steven A Hardy; Amy E Vincent; João Durães; Maria C Macário; Maria João Santos; Olinda Rebelo; Carla Lopes; João Pratas; Cândida Mendes; Mónica Zuzarte; A Cristina Rego; Henrique Girão; Lee-Jun C Wong; Robert W Taylor; Manuela Grazina
Journal:  Neuromuscul Disord       Date:  2017-11-23       Impact factor: 4.296

  9 in total

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