Attenuated clinical and osteoclastic phenotypes of Paget’s disease of bone linked to the p.Pro392Leu/SQSTM1 mutation by a rare variant in the DOCK6 gene

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作者
Mariam Dessay
Emile Couture
Halim Maaroufi
Frédéric Fournier
Edith Gagnon
Arnaud Droit
Jacques P. Brown
Laëtitia Michou
机构
[1] CHU de Québec-Université Laval Research Centre,Institut de Biologie Intégrative Et Des Systèmes (IBIS)
[2] Université Laval,Department of Medicine
[3] Université Laval,Department of Rheumatology
[4] CHU de Québec-Université Laval,R4774
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Paget’s disease of bone; gene; gene; p.Pro392Leu mutation; p.Val45Ile variant; Whole exome sequencing; Serum response factor;
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