A timeline of symptom onset and disease progression in CLN3 disease.

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Bibliographic Details
Title: A timeline of symptom onset and disease progression in CLN3 disease.
Authors: Whiteman IT; Batten Disease Support & Research Association Australia, 74 McLachlan Ave, Shelly Beach, NSW, 2261, Australia. research@bdsraaustralia.org.; Batten Disease Support, Research & Advocacy Foundation, Columbus, OH, USA. research@bdsraaustralia.org.; Beyond Batten Disease Foundation, Austin, TX, USA. research@bdsraaustralia.org., Cook AL; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia., Augustine EF; Kennedy Krieger Institute, Baltimore, MD, USA., Bindoff AD; Wicking Dementia Research and Education Centre, University of Tasmania, Tasmania, Australia., Johnson AM; Department of Neurology, Sydney Children's Hospital, University of New South Wales, Randwick, NSW, Australia., Mason HL; Coufetery Comms, Medical Writing Services, Mirepoix, France., Mink JW; Consultant, Pittsford, NY, USA., Østergaard JR; Centre for Rare Diseases, Aarhus University Hospital, Aarhus, Denmark., Schulz A; Children's Hospital, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.; German Center for Child and Adolescent Health (DZKJ), Partner Site Hamburg, Hamburg, Germany., Vermilion J; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA., Vierhile A; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA., Adams HR; Division of Child Neurology, Department of Neurology, University of Rochester Medical Center, Rochester, NY, USA.
Source: Orphanet journal of rare diseases [Orphanet J Rare Dis] 2026 Jan 07; Vol. 21 (1), pp. 38. Date of Electronic Publication: 2026 Jan 07.
Publication Type: Journal Article; Review
Journal Info: Publisher: BioMed Central Country of Publication: England NLM ID: 101266602 Publication Model: Electronic Cited Medium: Internet ISSN: 1750-1172 (Electronic) Linking ISSN: 17501172 NLM ISO Abbreviation: Orphanet J Rare Dis Subsets: MEDLINE
Database: MEDLINE Ultimate
Description
ISSN:1750-1172
DOI:10.1186/s13023-025-04174-5