Familial vs. sporadic sarcoidosis: BTNL2 polymorphisms, clinical presentations, and outcomes in a French cohort

被引:0
作者
Yves Pacheco
Alain Calender
Dominique Israël-Biet
Pascal Roy
Serge Lebecque
Vincent Cottin
Diane Bouvry
Hilario Nunes
Pascal Sève
Laurent Pérard
Gilles Devouassoux
Nathalie Freymond
Chahira Khouatra
Benoît Wallaert
Raphaelle Lamy
Mad-Hélénie Elsensohn
Claire Bardel
Dominique Valeyre
机构
[1] Université Claude Bernard – Lyon 1,Hospices Civils de Lyon, Centre Hospitalier Lyon Sud
[2] EA-7426,Hospices Civils de Lyon, Hôpital Edouard Herriot, Plateforme de génétique moléculaire, CR
[3] Université Claude Bernard - Lyon 1,21076
[4] INSERM U1052,AP
[5] Université René Descartes – Paris 5,HP, Hôpital Européen Georges Pompidou, Service de Pneumologie, Centre de Compétence des maladies pulmonaires rares
[6] Université Claude Bernard – Lyon 1,Hospices Civils de Lyon, Service de Biostatistique
[7] CNRS UMR 5558,Hospices Civils de Lyon, Hôpital Lyon
[8] Université Claude Bernard - Lyon1,Sud
[9] INSERM U1052 - CNRS UMR5286,Hospices Civils de Lyon, Hôpital Louis Pradel
[10] Université Claude Bernard - Lyon 1,AP
[11] UMR 754,HP, Hôpital Avicenne
[12] Université Paris13,Hospices Civils de Lyon, Hôpital Croix
[13] EA2363,Rousse
[14] COMUE Sorbonne Paris Cité,Hospices Civils de Lyon, Hôpital Edouard Herriot
[15] Université Claude Bernard - Lyon 1,Centre hospitalo
[16] Université Claude Bernard - Lyon 1,universitaire de Lille, Service de Pneumologie et Immunoallergologie, Centre de Compétence Maladies Pulmonaires Rares
[17] Université Lille 2,undefined
[18] Université Claude Bernard Lyon 1 - EA-7426,undefined
来源
Orphanet Journal of Rare Diseases | / 11卷
关键词
Sarcoidosis; Medical genetics; Human BTNL2 protein; Candidate gene association study; Classification;
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