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Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6

Detalles Bibliográficos
Autor principal: Finsterer, Josef
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Wolters Kluwer - Medknow 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666861/
https://www.ncbi.nlm.nih.gov/pubmed/38022443
http://dx.doi.org/10.4103/aian.aian_501_23
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author Finsterer, Josef
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spelling pubmed-106668612023-09-01 Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6 Finsterer, Josef Ann Indian Acad Neurol Letters to the Editor Wolters Kluwer - Medknow 2023 2023-10-05 /pmc/articles/PMC10666861/ /pubmed/38022443 http://dx.doi.org/10.4103/aian.aian_501_23 Text en Copyright: © 2023 Annals of Indian Academy of Neurology https://creativecommons.org/licenses/by-nc-sa/4.0/This is an open access journal, and articles are distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as appropriate credit is given and the new creations are licensed under the identical terms.
spellingShingle Letters to the Editor
Finsterer, Josef
Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title_full Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title_fullStr Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title_full_unstemmed Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title_short Double Trouble Myotonic Dystrophy Type-1 and Parkinson Syndrome Associated with Variants in SYNJI, VPS13C, and DNAJC6
title_sort double trouble myotonic dystrophy type-1 and parkinson syndrome associated with variants in synji, vps13c, and dnajc6
topic Letters to the Editor
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10666861/
https://www.ncbi.nlm.nih.gov/pubmed/38022443
http://dx.doi.org/10.4103/aian.aian_501_23
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