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Long-Read Sequencing Unravels the Complexity of Structural Variants in PRKN in Two Individuals with Early-Onset Parkinson's Disease.
Cogan, Guillaume; Daida, Kensuke; Billingsley, Kimberley J; Tesson, Christelle; Forlani, Sylvie; Jornea, Ludmila; Arnaud, Lionel; Tissier, Laurène; LeGuern, Eric; Singleton, Andrew B; Ferrien, Mélanie; Bernard, Hélène Gervais; Lesage, Suzanne; Blauwendraat, Cornelis; Brice, Alexis.
Affiliation
  • Cogan G; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
  • Daida K; Center for Alzheimer's and Related Dementias, National Institute on Aging, Bethesda, Maryland, USA.
  • Billingsley KJ; Institut National de la Recherche Médicale-U1127, Centre National de la Recherche Scientifique-UMR7225, APHP, Paris, France.
  • Tesson C; AP-HP Sorbonne Université, Département de génétique médicale, UF de Neurogénétique Moléculaire et Cellulaire, Hôpital Pitié-Salpêtrière, Paris, France.
  • Forlani S; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
  • Jornea L; Center for Alzheimer's and Related Dementias, National Institute on Aging, Bethesda, Maryland, USA.
  • Arnaud L; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
  • Tissier L; Center for Alzheimer's and Related Dementias, National Institute on Aging, Bethesda, Maryland, USA.
  • LeGuern E; Institut National de la Recherche Médicale-U1127, Centre National de la Recherche Scientifique-UMR7225, APHP, Paris, France.
  • Singleton AB; Institut National de la Recherche Médicale-U1127, Centre National de la Recherche Scientifique-UMR7225, APHP, Paris, France.
  • Ferrien M; Institut National de la Recherche Médicale-U1127, Centre National de la Recherche Scientifique-UMR7225, APHP, Paris, France.
  • Bernard HG; AP-HP Sorbonne Université, Département de génétique médicale, UF de Neurogénétique Moléculaire et Cellulaire, Hôpital Pitié-Salpêtrière, Paris, France.
  • Lesage S; AP-HP Sorbonne Université, Département de génétique médicale, UF de Neurogénétique Moléculaire et Cellulaire, Hôpital Pitié-Salpêtrière, Paris, France.
  • Blauwendraat C; AP-HP Sorbonne Université, Département de génétique médicale, UF de Neurogénétique Moléculaire et Cellulaire, Hôpital Pitié-Salpêtrière, Paris, France.
  • Brice A; Laboratory of Neurogenetics, National Institute on Aging, Bethesda, Maryland, USA.
Mov Disord ; 39(9): 1647-1648, 2024 Sep.
Article in En | MEDLINE | ID: mdl-38943243
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Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2024 Type: Article Affiliation country: United States
Fulltext
Print
XML
PubMed Links
Search on Google

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Mov Disord Journal subject: NEUROLOGIA Year: 2024 Type: Article Affiliation country: United States