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Novel Homozygous Pathogenic Variant in DNAJC6 Causes Rapid Progressive Parkinsonism.

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Title: Novel Homozygous Pathogenic Variant in DNAJC6 Causes Rapid Progressive Parkinsonism.
Authors: Pessoa ALS; Hospital Infantil Albert Sabin, Fortaleza, Brazil., Guimarães TG; Department of Neurology, Movement Disorders Center, University of Sao Paulo, Sao Paulo, Brazil.; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil., de Castro Dos Santos D; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil., Barbosa RMG; Department of Neurology, Movement Disorders Center, University of Sao Paulo, Sao Paulo, Brazil.; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil., Lopes EMS; Hospital Infantil Albert Sabin, Fortaleza, Brazil., de Gusmao CM; Department of Neurology, Mass General Brigham, Harvard Medical School, Boston, Massachusetts, USA., Lima PLGSB; Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Brazil., Castro MAA; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil., Kok F; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil., Nobrega PR; Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Brazil.
Source: Movement disorders clinical practice [Mov Disord Clin Pract] 2026 Jul 07. Date of Electronic Publication: 2026 Jul 07.
Publication Type: Journal Article; Review
Journal Info: Publisher: Wiley Country of Publication: United States NLM ID: 101630279 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 2330-1619 (Electronic) Linking ISSN: 23301619 NLM ISO Abbreviation: Mov Disord Clin Pract Subsets: MEDLINE
Database: MEDLINE Ultimate
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  Data: Novel Homozygous Pathogenic Variant in DNAJC6 Causes Rapid Progressive Parkinsonism.
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  Data: <searchLink fieldCode="AU" term="%22Pessoa+ALS%22">Pessoa ALS</searchLink>; Hospital Infantil Albert Sabin, Fortaleza, Brazil.<br /><searchLink fieldCode="AU" term="%22Guimarães+TG%22">Guimarães TG</searchLink>; Department of Neurology, Movement Disorders Center, University of Sao Paulo, Sao Paulo, Brazil.; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22de+Castro+Dos+Santos+D%22">de Castro Dos Santos D</searchLink>; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Barbosa+RMG%22">Barbosa RMG</searchLink>; Department of Neurology, Movement Disorders Center, University of Sao Paulo, Sao Paulo, Brazil.; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Lopes+EMS%22">Lopes EMS</searchLink>; Hospital Infantil Albert Sabin, Fortaleza, Brazil.<br /><searchLink fieldCode="AU" term="%22de+Gusmao+CM%22">de Gusmao CM</searchLink>; Department of Neurology, Mass General Brigham, Harvard Medical School, Boston, Massachusetts, USA.<br /><searchLink fieldCode="AU" term="%22Lima+PLGSB%22">Lima PLGSB</searchLink>; Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Brazil.<br /><searchLink fieldCode="AU" term="%22Castro+MAA%22">Castro MAA</searchLink>; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Kok+F%22">Kok F</searchLink>; Department of Neurology, Neurogenetics Center, University of São Paulo, Sao Paulo, Brazil.<br /><searchLink fieldCode="AU" term="%22Nobrega+PR%22">Nobrega PR</searchLink>; Division of Neurology, Department of Clinical Medicine, Universidade Federal do Ceará, Fortaleza, Brazil.
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  Data: <i>Publisher: </i><searchLink fieldCode="PB" term="%22Wiley%22">Wiley </searchLink><i>Country of Publication: </i>United States <i>NLM ID: </i>101630279 <i>Publication Model: </i>Print-Electronic <i>Cited Medium: </i>Internet <i>ISSN: </i>2330-1619 (Electronic) <i>Linking ISSN: </i><searchLink fieldCode="IS" term="%2223301619%22">23301619 </searchLink><i>NLM ISO Abbreviation: </i>Mov Disord Clin Pract <i>Subsets: </i>MEDLINE
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        Value: 10.1002/mdc3.70731
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        Text: English
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      – TitleFull: Novel Homozygous Pathogenic Variant in DNAJC6 Causes Rapid Progressive Parkinsonism.
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            – D: 07
              M: 07
              Text: 2026 Jul 07
              Type: published
              Y: 2026
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