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FARS2 Causing Complex Hereditary Spastic Paraplegia With Dysphonia: Expanding the Disease Spectrum.

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Title: FARS2 Causing Complex Hereditary Spastic Paraplegia With Dysphonia: Expanding the Disease Spectrum.
Authors: Forman EB; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland., Gorman KM; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland., Ennis S; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland., King MD; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland.
Source: Journal of child neurology [J Child Neurol] 2019 Sep; Vol. 34 (10), pp. 621. Date of Electronic Publication: 2019 May 19.
Publication Type: Case Reports; Letter
Journal Info: Publisher: Sage Country of Publication: United States NLM ID: 8606714 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1708-8283 (Electronic) Linking ISSN: 08830738 NLM ISO Abbreviation: J Child Neurol Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: FARS2 Causing Complex Hereditary Spastic Paraplegia With Dysphonia: Expanding the Disease Spectrum.
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  Data: <searchLink fieldCode="AU" term="%22Forman+EB%22">Forman EB</searchLink>; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland.<br /><searchLink fieldCode="AU" term="%22Gorman+KM%22">Gorman KM</searchLink>; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland.<br /><searchLink fieldCode="AU" term="%22Ennis+S%22">Ennis S</searchLink>; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland.<br /><searchLink fieldCode="AU" term="%22King+MD%22">King MD</searchLink>; Department of Neurology and Neurophysiology, Children's University Hospital, Dublin, Ireland.; Academic Centre on Rare Disease (ACoRD), University College Dublin, Ireland.
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  Data: <searchLink fieldCode="JN" term="%228606714%22">Journal of child neurology</searchLink> [J Child Neurol] 2019 Sep; Vol. 34 (10), pp. 621. <i>Date of Electronic Publication: </i>2019 May 19.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Sage%22">Sage </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>8606714 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>1708-8283 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2208830738%22">08830738 </searchLink><i>NLM ISO Abbreviation: </i>J Child Neurol <i>Subsets: </i>MEDLINE
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              Text: 2019 Sep
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