Search Results - Frédéric Fournier
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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 by Mariam Dessay, Emile Couture, Halim Maaroufi, Frédéric Fournier, Edith Gagnon, Arnaud Droit, Jacques P. Brown, Laëtitia Michou
Published 2022Call Number: Loading…Connect to this object online.
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