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ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.

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Title: ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.
Authors: Rohrbach M; Division of Metabolism, Connective Tissue Unit and Children's Research Center, University Children's Hospital, Zurich, Switzerland., Spencer HL, Porter LF, Burkitt-Wright EM, Bürer C, Janecke A, Bakshi M, Sillence D, Al-Hussain H, Baumgartner M, Steinmann B, Black GC, Manson FD, Giunta C
Source: Molecular genetics and metabolism [Mol Genet Metab] 2013 Jul; Vol. 109 (3), pp. 289-95. Date of Electronic Publication: 2013 Apr 26.
Publication Type: Journal Article; Research Support, Non-U.S. Gov't
Journal Info: Publisher: Academic Press Country of Publication: United States NLM ID: 9805456 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1096-7206 (Electronic) Linking ISSN: 10967192 NLM ISO Abbreviation: Mol Genet Metab Subsets: MEDLINE
Database: MEDLINE Ultimate
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An: 23680354
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PubType: Academic Journal
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  Data: ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.
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  Data: <searchLink fieldCode="AU" term="%22Rohrbach+M%22">Rohrbach M</searchLink>; Division of Metabolism, Connective Tissue Unit and Children's Research Center, University Children's Hospital, Zurich, Switzerland.<br /><searchLink fieldCode="AU" term="%22Spencer+HL%22">Spencer HL</searchLink><br /><searchLink fieldCode="AU" term="%22Porter+LF%22">Porter LF</searchLink><br /><searchLink fieldCode="AU" term="%22Burkitt-Wright+EM%22">Burkitt-Wright EM</searchLink><br /><searchLink fieldCode="AU" term="%22Bürer+C%22">Bürer C</searchLink><br /><searchLink fieldCode="AU" term="%22Janecke+A%22">Janecke A</searchLink><br /><searchLink fieldCode="AU" term="%22Bakshi+M%22">Bakshi M</searchLink><br /><searchLink fieldCode="AU" term="%22Sillence+D%22">Sillence D</searchLink><br /><searchLink fieldCode="AU" term="%22Al-Hussain+H%22">Al-Hussain H</searchLink><br /><searchLink fieldCode="AU" term="%22Baumgartner+M%22">Baumgartner M</searchLink><br /><searchLink fieldCode="AU" term="%22Steinmann+B%22">Steinmann B</searchLink><br /><searchLink fieldCode="AU" term="%22Black+GC%22">Black GC</searchLink><br /><searchLink fieldCode="AU" term="%22Manson+FD%22">Manson FD</searchLink><br /><searchLink fieldCode="AU" term="%22Giunta+C%22">Giunta C</searchLink>
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  Data: <searchLink fieldCode="JN" term="%229805456%22">Molecular genetics and metabolism</searchLink> [Mol Genet Metab] 2013 Jul; Vol. 109 (3), pp. 289-95. <i>Date of Electronic Publication: </i>2013 Apr 26.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Academic+Press%22">Academic Press </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>9805456 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1096-7206 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2210967192%22">10967192 </searchLink><i>NLM ISO Abbreviation: </i>Mol Genet Metab <i>Subsets: </i>MEDLINE
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        Value: 10.1016/j.ymgme.2013.04.014
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      – Code: eng
        Text: English
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        StartPage: 289
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      – TitleFull: ZNF469 frequently mutated in the brittle cornea syndrome (BCS) is a single exon gene possibly regulating the expression of several extracellular matrix components.
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              Text: 2013 Jul
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