Laugwitz, L., Martin, P., Janzen, N., Hegert, S., Neiße, T., Wacker, M., . . . Groeschel, S. (2026). Clinical management of metachromatic leukodystrophy cases identified in the German and Austrian Newborn screening pilots. Orphanet Journal of Rare Diseases, 21(1), . https://doi.org/10.1186/s13023-026-04620-y
Παραπομπή σε μορφή Chicago (17η εκδ.)Laugwitz, Lucia, et al. "Clinical Management of Metachromatic Leukodystrophy Cases Identified in the German and Austrian Newborn Screening Pilots." Orphanet Journal of Rare Diseases 21, no. 1 (2026). https://doi.org/10.1186/s13023-026-04620-y.
Παραπομπή σε μορφή MLA (9th εκδ.)Laugwitz, Lucia, et al. "Clinical Management of Metachromatic Leukodystrophy Cases Identified in the German and Austrian Newborn Screening Pilots." Orphanet Journal of Rare Diseases, vol. 21, no. 1, 2026, https://doi.org/10.1186/s13023-026-04620-y.