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Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration Volume 14, 2013 - Issue 7-8
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Case Reports

Late adult-onset pure spinal muscular atrophy due to a compound HEXB macro-deletion

Tim W. RattayDepartment of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen;German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen
,
Ludger SchölsDepartment of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen;German Research Centre for Neurodegenerative Diseases (DZNE), Tübingen
,
Christian WilhelmCeGaT GmbH, Centre for Genomics and Transcriptomics, Tübingen, Germany
&
Matthis SynofzikDepartment of Neurodegenerative Diseases, Hertie-Institute for Clinical Brain Research, University of Tübingen;German Research Centre for Neurodegenerative Diseases (DZNE), TübingenCorrespondence[email protected]
Pages 628-629 | Received 01 May 2013, Accepted 04 Jun 2013, Published online: 25 Jul 2013

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Leidy García Morales, Reinaldo Gaspar Mustelier Bécquer, Laura Pérez Joglar & Tatiana Zaldívar Vaillant. (2022) Sandhoff disease in the elderly: a case study . Amyotrophic Lateral Sclerosis and Frontotemporal Degeneration 23:1-2, pages 137-138.
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Articles from other publishers (3)

R. Juntas Morales, N. Pageot, G. Taieb & W. Camu. (2017) Adult-onset spinal muscular atrophy: An update. Revue Neurologique 173:5, pages 308-319.
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Jodi Warman Chardon, Pierre R. Bourque, Michael T. Geraghty & Kym M. Boycott. (2015) Very late-onset Sandhoff disease presenting as Kennedy Disease. Muscle & Nerve 52:6, pages 1135-1136.
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Kristien Peeters, Teodora Chamova & Albena Jordanova. (2014) Clinical and genetic diversity of SMN1-negative proximal spinal muscular atrophies. Brain 137:11, pages 2879-2896.
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