Lista publicaţiilor: Orphanet Journal of Rare Diseases. Descărcări - 1. Vizualizări - 713.2017 - 1
Genotype-phenotype correlations and expansion of the molecular spectrum of AP4M1-related hereditary spastic paraplegia |
Bettencourt C., Salpietro Vincenzo, Efthymiou Stephanie, Chelban Viorica, Hughes Deborah, Houlden Henry H., Federoff Monica, Bourinaris Thomas, Spilioti Martha G, Deretzi Georgia, Kalantzakou Triantafyllia, Singleton Andrew B., Xiromerisiou Georgia |
1 University College London, 2 ”Nicolae Testemițanu” State University of Medicine and Pharmacy, 3 National Institute on Aging, National Institutes of Health, Bethesda, 4 Papageorgiou Hospital, Thessaloniki, 5 University of Thessaloniki, AHEPA University Hospital, Thessaloniki |
Orphanet Journal of Rare Diseases |
Nr. 1(12) / 2017 / ISSN 1750-1172 |
Disponibil online 11 December, 2017. Descarcări-1. Vizualizări-713 |
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