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The Clinical Utility of Determining the Allelic Background of Mutations Causing Alpha-1 Antitrypsin Deficiency: The Case with the Null Variant Q0(Mattawa)/Q0(Ourém).
Chronic Obstr Pulm Dis. 2021 Jan;8(1):31-40. doi: 10.15326/jcopdf.8.1.2020.0168.
Chronic Obstr Pulm Dis. 2021.
PMID: 33150777
Free PMC article.
Prioritization of candidate causal genes for asthma in susceptibility loci derived from UK Biobank.
Valette K, Li Z, Bon-Baret V, Chignon A, Bérubé JC, Eslami A, Lamothe J, Gaudreault N, Joubert P, Obeidat M, van den Berge M, Timens W, Sin DD, Nickle DC, Hao K, Labbé C, Godbout K, Côté A, Laviolette M, Boulet LP, Mathieu P, Thériault S, Bossé Y.
Valette K, et al.
Commun Biol. 2021 Jun 8;4(1):700. doi: 10.1038/s42003-021-02227-6.
Commun Biol. 2021.
PMID: 34103634
Free PMC article.
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[Computed tomography lung density and small vessel quantification in pulmonary hypertension associated with progressive fibrosing interstitial lung disease (PF-ILD)].
Valette K, Bermudez J, Habert P, Puech B, Gaubert JY, Reynaud-Gaubert M, Coiffard B.
Valette K, et al.
Rev Mal Respir. 2022 Mar;39(3):199-211. doi: 10.1016/j.rmr.2021.11.003. Epub 2022 Feb 24.
Rev Mal Respir. 2022.
PMID: 35221162
French.
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