O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium
Titel:
O36: Long-read genome sequencing in unsolved rare genetic diseases: Preliminary experiences from the Care4Rare Canada Consortium
Auteur:
Del Gobbo, Giulia Couse, Madeline Lambert, Christine Zhang, Siyuan Dhillon, Harsharan Fanslow, Cairbre Rowell, William Dolzhenko, Egor De Sena Brandine, Guilherme Eberle, Michael Marshall, Christian Kernohan, Kristin Boycott, Kym