Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.

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Title: Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
Authors: Gast C; Wessex Kidney Centre, Portsmouth Hospitals NHS Trust, Portsmouth, UK Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK., Pengelly RJ; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK., Lyon M; Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, UK., Bunyan DJ; Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, UK., Seaby EG; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK., Graham N; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK., Venkat-Raman G; Wessex Kidney Centre, Portsmouth Hospitals NHS Trust, Portsmouth, UK., Ennis S; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.
Source: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association [Nephrol Dial Transplant] 2016 Jun; Vol. 31 (6), pp. 961-70. Date of Electronic Publication: 2015 Sep 07.
Publication Type: Journal Article
Journal Info: Publisher: Oxford University Press Country of Publication: England NLM ID: 8706402 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1460-2385 (Electronic) Linking ISSN: 09310509 NLM ISO Abbreviation: Nephrol Dial Transplant Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
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  Data: <searchLink fieldCode="AU" term="%22Gast+C%22">Gast C</searchLink>; Wessex Kidney Centre, Portsmouth Hospitals NHS Trust, Portsmouth, UK Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.<br /><searchLink fieldCode="AU" term="%22Pengelly+RJ%22">Pengelly RJ</searchLink>; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.<br /><searchLink fieldCode="AU" term="%22Lyon+M%22">Lyon M</searchLink>; Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, UK.<br /><searchLink fieldCode="AU" term="%22Bunyan+DJ%22">Bunyan DJ</searchLink>; Wessex Regional Genetics Laboratory, Salisbury District Hospital, Salisbury, UK.<br /><searchLink fieldCode="AU" term="%22Seaby+EG%22">Seaby EG</searchLink>; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.<br /><searchLink fieldCode="AU" term="%22Graham+N%22">Graham N</searchLink>; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.<br /><searchLink fieldCode="AU" term="%22Venkat-Raman+G%22">Venkat-Raman G</searchLink>; Wessex Kidney Centre, Portsmouth Hospitals NHS Trust, Portsmouth, UK.<br /><searchLink fieldCode="AU" term="%22Ennis+S%22">Ennis S</searchLink>; Human Genetics and Genomic Medicine, Faculty of Medicine, University of Southampton, Southampton, UK.
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  Data: <searchLink fieldCode="JN" term="%228706402%22">Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association</searchLink> [Nephrol Dial Transplant] 2016 Jun; Vol. 31 (6), pp. 961-70. <i>Date of Electronic Publication: </i>2015 Sep 07.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Oxford+University+Press%22">Oxford University Press </searchLink><i>Country of Publication: </i>England <i>NLM ID: </i>8706402 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1460-2385 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2209310509%22">09310509 </searchLink><i>NLM ISO Abbreviation: </i>Nephrol Dial Transplant <i>Subsets: </i>MEDLINE
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      – Type: doi
        Value: 10.1093/ndt/gfv325
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      – Code: eng
        Text: English
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      – TitleFull: Collagen (COL4A) mutations are the most frequent mutations underlying adult focal segmental glomerulosclerosis.
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              Text: 2016 Jun
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              Y: 2016
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            – TitleFull: Nephrology, dialysis, transplantation : official publication of the European Dialysis and Transplant Association - European Renal Association
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