ATXN10 and facioscapulohumeral muscular dystrophy: (Ardui et al., 2018) For example, the telomere-to-telomere (T2T) consortium has applied this technology for CHM13 genome sequence assembly, as well as for detecting mutations causing for facioscapulohumeral muscular dystrophy (FSHD), SCA10, and other diseases.