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Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.

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Title: Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
Authors: Feigenbaum A; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada., Bai RK, Doherty ES, Kwon H, Tan D, Sloane A, Cutz E, Robinson BH, Wong LJ
Source: American journal of medical genetics. Part A [Am J Med Genet A] 2006 Oct 15; Vol. 140 (20), pp. 2216-22.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Wiley-Blackwell Country of Publication: United States NLM ID: 101235741 Publication Model: Print Cited Medium: Print ISSN: 1552-4825 (Print) Linking ISSN: 15524825 NLM ISO Abbreviation: Am J Med Genet A Subsets: MEDLINE
Database: MEDLINE Ultimate
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PubType: Academic Journal
PubTypeId: academicJournal
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  Data: Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
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  Data: <searchLink fieldCode="AU" term="%22Feigenbaum+A%22">Feigenbaum A</searchLink>; Division of Clinical and Metabolic Genetics, The Hospital for Sick Children, Toronto, Ontario, Canada.<br /><searchLink fieldCode="AU" term="%22Bai+RK%22">Bai RK</searchLink><br /><searchLink fieldCode="AU" term="%22Doherty+ES%22">Doherty ES</searchLink><br /><searchLink fieldCode="AU" term="%22Kwon+H%22">Kwon H</searchLink><br /><searchLink fieldCode="AU" term="%22Tan+D%22">Tan D</searchLink><br /><searchLink fieldCode="AU" term="%22Sloane+A%22">Sloane A</searchLink><br /><searchLink fieldCode="AU" term="%22Cutz+E%22">Cutz E</searchLink><br /><searchLink fieldCode="AU" term="%22Robinson+BH%22">Robinson BH</searchLink><br /><searchLink fieldCode="AU" term="%22Wong+LJ%22">Wong LJ</searchLink>
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  Data: <searchLink fieldCode="JN" term="%22101235741%22">American journal of medical genetics. Part A</searchLink> [Am J Med Genet A] 2006 Oct 15; Vol. 140 (20), pp. 2216-22.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley-Blackwell%22">Wiley-Blackwell </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101235741 <i>Publication Model: </i>Print <i>Cited Medium: </i>Print <i>ISSN: </i>1552-4825 (Print) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2215524825%22">15524825 </searchLink><i>NLM ISO Abbreviation: </i>Am J Med Genet A <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1002/ajmg.a.31436
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      – Code: eng
        Text: English
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        StartPage: 2216
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      – TitleFull: Novel mitochondrial DNA mutations associated with myopathy, cardiomyopathy, renal failure, and deafness.
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            NameFull: Feigenbaum A
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            NameFull: Bai RK
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            – D: 15
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              Text: 2006 Oct 15
              Type: published
              Y: 2006
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              Value: 140
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              Value: 20
          Titles:
            – TitleFull: American journal of medical genetics. Part A
              Type: main
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