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Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation.

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Title: Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation.
Authors: Gentil C; UM76-UPMC/U974-Inserm/UMR7215-CNRS, Institut de Myologie 105 Bd de l’Hôpital, 75013 Paris, France., Leturcq F, Ben Yaou R, Kaplan JC, Laforet P, Pénisson-Besnier I, Espil-Taris C, Voit T, Garcia L, Piétri-Rouxel F
Source: Human molecular genetics [Hum Mol Genet] 2012 Aug 01; Vol. 21 (15), pp. 3449-60. Date of Electronic Publication: 2012 May 15.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: IRL Press at Oxford University Press Country of Publication: England NLM ID: 9208958 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2083 (Electronic) Linking ISSN: 09646906 NLM ISO Abbreviation: Hum Mol Genet Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Variable phenotype of del45-55 Becker patients correlated with nNOSμ mislocalization and RYR1 hypernitrosylation.
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  Data: <searchLink fieldCode="AU" term="%22Gentil+C%22">Gentil C</searchLink>; UM76-UPMC/U974-Inserm/UMR7215-CNRS, Institut de Myologie 105 Bd de l’Hôpital, 75013 Paris, France.<br /><searchLink fieldCode="AU" term="%22Leturcq+F%22">Leturcq F</searchLink><br /><searchLink fieldCode="AU" term="%22Ben+Yaou+R%22">Ben Yaou R</searchLink><br /><searchLink fieldCode="AU" term="%22Kaplan+JC%22">Kaplan JC</searchLink><br /><searchLink fieldCode="AU" term="%22Laforet+P%22">Laforet P</searchLink><br /><searchLink fieldCode="AU" term="%22Pénisson-Besnier+I%22">Pénisson-Besnier I</searchLink><br /><searchLink fieldCode="AU" term="%22Espil-Taris+C%22">Espil-Taris C</searchLink><br /><searchLink fieldCode="AU" term="%22Voit+T%22">Voit T</searchLink><br /><searchLink fieldCode="AU" term="%22Garcia+L%22">Garcia L</searchLink><br /><searchLink fieldCode="AU" term="%22Piétri-Rouxel+F%22">Piétri-Rouxel F</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229208958%22">Human molecular genetics</searchLink> [Hum Mol Genet] 2012 Aug 01; Vol. 21 (15), pp. 3449-60. <i>Date of Electronic Publication: </i>2012 May 15.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22IRL+Press+at+Oxford+University+Press%22">IRL Press at Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>9208958 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2083 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209646906%22">09646906 </searchLink><i>NLM ISO Abbreviation: </i>Hum Mol Genet <i>Subsets: </i>MEDLINE
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        Value: 10.1093/hmg/dds176
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              Text: 2012 Aug 01
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