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Molecular and Phenotypic Characterization of the RORB-Related Disorder.
Neurology. 2024 Jan 23;102(2):e207945. doi: 10.1212/WNL.0000000000207945. Epub 2023 Dec 22.
Neurology. 2024.
PMID: 38165337
The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care.
De Antonio M, Dogan C, Daidj F, Eymard B, Puymirat J, Mathieu J, Gagnon C, Katsahian S; Filnemus Myotonic Dystrophy Study Group; Hamroun D, Bassez G.
De Antonio M, et al.
Orphanet J Rare Dis. 2019 Jun 3;14(1):122. doi: 10.1186/s13023-019-1088-3.
Orphanet J Rare Dis. 2019.
PMID: 31159885
Free PMC article.
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