Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia.
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| Title: | Novel Genetic, Clinical, and Pathomechanistic Insights into TFG-Associated Hereditary Spastic Paraplegia. |
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| Authors: | Harlalka GV; University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK., McEntagart ME; Medical Genetics Unit, Floor 0, Jenner Wing, St. George's University of London, Cranmer Terrace, London, UK., Gupta N; Division of Genetics, Department of Pediatrics, Old O.T. Block, All India Institute of Medical Sciences, New Delhi, India., Skrzypiec AE; Laboratory of Neuronal Plasticity and Behaviour, University of Exeter Medical School, University of Exeter, Exeter, UK., Mucha MW; Laboratory of Neuronal Plasticity and Behaviour, University of Exeter Medical School, University of Exeter, Exeter, UK., Chioza BA; University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK., Simpson MA; Division of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's Hospital, London, UK., Sreekantan-Nair A; University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK., Pereira A; Department of Neurology, Atkinson Morley Wing, St. George's Hospital, Tooting, London, UK., Günther S; Department of Clinical Chemistry and Laboratory Medicine, Jena University Hospital, Jena, Germany., Jahic A; Department of Clinical Chemistry and Laboratory Medicine, Jena University Hospital, Jena, Germany., Modarres H; Department of Neurology, Atkinson Morley Wing, St. George's Hospital, Tooting, London, UK., Moore-Barton H; Medical Genetics Unit, Floor 0, Jenner Wing, St. George's University of London, Cranmer Terrace, London, UK., Trembath RC; Division of Genetics and Molecular Medicine, King's College London School of Medicine, Guy's Hospital, London, UK., Kabra M; Division of Genetics, Department of Pediatrics, Old O.T. Block, All India Institute of Medical Sciences, New Delhi, India., Baple EL; University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK., Thakur S; Department of Genetics and Fetal Medicine, Fortis La femme, S-549, New Delhi, India., Patton MA; Medical Genetics Unit, Floor 0, Jenner Wing, St. George's University of London, Cranmer Terrace, London, UK., Beetz C; Department of Clinical Chemistry and Laboratory Medicine, Jena University Hospital, Jena, Germany. christian.beetz@med.uni.jena.de., Pawlak R; Laboratory of Neuronal Plasticity and Behaviour, University of Exeter Medical School, University of Exeter, Exeter, UK., Crosby AH; University of Exeter Medical School, RILD Wellcome Wolfson Centre, Royal Devon & Exeter NHS Foundation Trust, Barrack Road, Exeter, UK. |
| Source: | Human mutation [Hum Mutat] 2016 Nov; Vol. 37 (11), pp. 1157-1161. Date of Electronic Publication: 2016 Aug 30. |
| Publication Type: | Journal Article; Research Support, Non-U.S. Gov't |
| Journal Info: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 9215429 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1098-1004 (Electronic) Linking ISSN: 10597794 NLM ISO Abbreviation: Hum Mutat Subsets: MEDLINE |
| Database: | MEDLINE Ultimate |
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