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pro vyhledávání: '"Hayden Michael R"'
Autor:
Squitieri F; Huntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Research Hospital, San Giovanni Rotondo, Italy. f.squitieri@css-mendel.it., Mazza T; Bioinformatics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Research Hospital, San Giovanni Rotondo, Italy., Maffi S; Huntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Research Hospital, San Giovanni Rotondo, Italy., De Luca A; Medical Genetics Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Research Hospital, San Giovanni Rotondo, Italy., AlSalmi Q; National Genetic Centre, Royal Hospital, Ministry of Health, Muscat, Sultanate of Oman., AlHarasi S; National Genetic Centre, Royal Hospital, Ministry of Health, Muscat, Sultanate of Oman., Collins JA; Centre for Molecular Medicine Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada., Kay C; Centre for Molecular Medicine Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada., Baine-Savanhu F; NHLS & School of Pathology, University of the Witwatersrand, Johannesburg, South Africa., Landwhermeyer BG; Abteilung Neurologie, Universitätsklinik Ulm, Ulm, Germany., Sabatini U; Department of Neuroradiology, University Magna Graecia, Catanzaro, Italy.; Italian League for Research on Huntington Disease (LIRH) Foundation, Rome, Italy., Hayden MR; Centre for Molecular Medicine Therapeutics, Department of Medical Genetics, University of British Columbia, Vancouver, BC, Canada.
Publikováno v:
Genetics in medicine : official journal of the American College of Medical Genetics [Genet Med] 2020 Nov; Vol. 22 (11), pp. 1903-1908. Date of Electronic Publication: 2020 Jul 14.