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Launching a multi-level data strategy for rare eye diseases: a methodological case study from national to European scale
Jul 21, 2026
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Orphanet Journal of Rare Diseases
Orphanet Journal of Rare Diseases
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Molecular basis of sarcomeric variants and the modifying role of non-sarcomeric genes in Sudden unexplained nocturnal death syndrome (SUNDS)
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Eating behaviour phenotype in the MYT1L-related neurodevelopmental disorder: a deep phenotyping study using standardized questionnaires
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