A pathogenic deletion in Forkhead Box L1 (FOXL1) identifies the first otosclerosis (OTSC) gene

Nelly Abdelfatah(Memorial University of Newfoundland), Terry‐Lynn Young(Memorial University of Newfoundland), Tammy Benteau(Memorial University of Newfoundland), Christopher Rowley(Memorial University of Newfoundland), Lance P. Doucette(Memorial University of Newfoundland), Sumit Agrawal(Western University), Tony Batten, Nanna Dahl Rendtorff(Rigshospitalet), Danielle French(Memorial University of Newfoundland), Pingzhao Hu(University of Manitoba), Susan G. Stanton(Western University), Kathy Hodgkinson(St. Mary’s Hospital), Darren D. O’Rielly(Memorial University of Newfoundland), Jessica E. Besaw(University of Toronto), Leichelle Little(Western University), Cindy Penney(Memorial University of Newfoundland), Anne Griffin(Memorial University of Newfoundland), Dante Galutira(Memorial University of Newfoundland), Justin A. Pater(Memorial University of Newfoundland), Valerie Booth(Memorial University of Newfoundland), Lorne Parnes(London Health Sciences Centre), Jim Houston(Memorial University of Newfoundland), Lisbeth Tranebjærg(UiT The Arctic University of Norway), Matthew B. Lucas(Western University), Susan Moore(Memorial University of Newfoundland), Ahmed Mostafa(Memorial University of Newfoundland), Courtney MacDonald(Memorial University of Newfoundland), Curtis R. French(Memorial University of Newfoundland)
Human Genetics
October 11, 2021
Cited by 15


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