Literature DB >> 2652392

Mitochondrial DNA mutations and neuromuscular disease.

D C Wallace.   

Abstract

Mitochondrial DNA mutations have been identified in patients with certain neuromuscular diseases. Point mutations have been associated with maternally inherited diseases, while deletions have been identified in some 'spontaneous' cases.

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Year:  1989        PMID: 2652392     DOI: 10.1016/0168-9525(89)90005-x

Source DB:  PubMed          Journal:  Trends Genet        ISSN: 0168-9525            Impact factor:   11.639


  50 in total

1.  Detection of a specific mitochondrial DNA deletion in tissues of older humans.

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Journal:  Plant Cell       Date:  1993-10       Impact factor: 11.277

5.  Identification of human remains by amplification and automated sequencing of mitochondrial DNA.

Authors:  K M Sullivan; R Hopgood; P Gill
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Authors:  A Rötig; V Cormier; S Blanche; J P Bonnefont; F Ledeist; N Romero; J Schmitz; P Rustin; A Fischer; J M Saudubray
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8.  Departure of human mitochondrial DNA variation from neutral expectations: an alternative explanation.

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9.  Detection of "deleted" mitochondrial genomes in cytochrome-c oxidase-deficient muscle fibers of a patient with Kearns-Sayre syndrome.

Authors:  S Mita; B Schmidt; E A Schon; S DiMauro; E Bonilla
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10.  Partial outlet obstruction of the rabbit bladder results in changes in the mitochondrial genetic system.

Authors:  Y Zhao; R M Levin; S S Levin; C A Nevel; N Haugaard; T H Hsu; A P Hudson
Journal:  Mol Cell Biochem       Date:  1994-12-07       Impact factor: 3.396

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