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    Source: Seefried, L, Aliberti, F, Heier, C A, Arango-Sancho, P, Biosse Duplan, M, Sakka, S D, Emma, F, Gardiner, O, Javaid, M K, Ferreira-Santos, R M, Raimann, A, Rak, K, Bubbear, J S, Cheung, M S, Beck-Nielsen, S S, Mindler, G T & Linglart, A 2025, 'XLH Matters : an evolving programme to discuss new advances and share clinical experiences to improve patient outcomes', Orphanet Journal of Rare Diseases, vol. 19, no. Supplement 2, 497. https://doi.org/10.1186/s13023-024-03387-4

    Relation: info:eu-repo/semantics/altIdentifier/pmid/39901153; info:eu-repo/semantics/altIdentifier/pissn/1750-1172; info:eu-repo/semantics/altIdentifier/eissn/1750-1172

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