Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration.
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| Title: | Deficiency of the zinc finger protein ZFP106 causes motor and sensory neurodegeneration. |
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| Authors: | Joyce PI; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Fratta P; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Landman AS; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Mcgoldrick P; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Wackerhage H; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Groves M; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Busam BS; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Galino J; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Corrochano S; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Beskina OA; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Esapa C; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Ryder E; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Carter S; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Stewart M; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Codner G; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Hilton H; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Teboul L; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Tucker J; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK., Lionikas A; Health Sciences, University of Aberdeen, Aberdeen AB25 2ZD, UK., Estabel J; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., Ramirez-Solis R; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., White JK; Sanger Institute, Wellcome Trust Genome Campus, Hinxton, Cambridgeshire CB10 1SA, UK and., Brandner S; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Plagnol V; UCL Genetics Institute, London WC1E 6BT, UK., Bennet DL; Nuffield Department of Clinical Neurosciences, University of Oxford, Oxford OX3 9DU, UK., Abramov AY; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK., Greensmith L; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk., Fisher EM; UCL Institute of Neurology and MRC Centre for Neuromuscular Disease, Queen Square, London WC1N 3BG, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk., Acevedo-Arozena A; MRC Mammalian Genetics Unit, Harwell, Oxfordshire OX11 0RD, UK, a.acevedo@har.mrc.ac.uk e.fisher@prion.ucl.ac.uk l.greensmith@ucl.ac.uk. |
| Source: | Human molecular genetics [Hum Mol Genet] 2016 Jan 15; Vol. 25 (2), pp. 291-307. Date of Electronic Publication: 2015 Nov 24. |
| 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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