The recurrent homozygous translation start site variant in CCDC134 in an individual with severe osteogenesis imperfecta of non-Morrocan ancestry - Ali, Taccyanna M.; Linnenkamp, Bianca D. W.; Yamamoto, Guilherme L.; Honjo, Rachel S.; Menezes Filho, Hamilton Cabral de; Kim, Chong Ae; Bertola, Debora R. (American journal of medical genetics part a, 2022)