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	MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosis
	Bonella, Francesco*; Long, Xiaoping; Ohshimo, Shinichiro; Horimasu, Yasushi; Griese, Matthias; Guzman, Josune; Kohno, Nobuoki; Costabel, Ulrich
刊名	Orphanet Journal of Rare Diseases
	2016
卷号	11期号:1页码:48
关键词	Disease outcome KL-6 MUC1 polymorphisms Pulmonary alveolar proteinosis
ISSN号	1750-1172
DOI	10.1186/s13023-016-0430-2
URL标识	查看原文
WOS记录号	WOS:000374653100001
内容类型	期刊论文
URI标识	http://www.corc.org.cn/handle/1471x/5678671
专题	南华大学
作者单位	1.[Bonella, Francesco 2.Long, Xiaoping 3.Costabel, Ulrich] Univ Duisburg Essen, Interstitial & Rare Lung Dis Unit, Ruhrlandklin, D-45239 Essen, Germany.
推荐引用方式 GB/T 7714	Bonella, Francesco*,Long, Xiaoping,Ohshimo, Shinichiro,et al. MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosis[J]. Orphanet Journal of Rare Diseases,2016,11(1):48.
APA	Bonella, Francesco*.,Long, Xiaoping.,Ohshimo, Shinichiro.,Horimasu, Yasushi.,Griese, Matthias.,...&Costabel, Ulrich.(2016).MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosis.Orphanet Journal of Rare Diseases,11(1),48.
MLA	Bonella, Francesco*,et al."MUC1 gene polymorphisms are associated with serum KL-6 levels and pulmonary dysfunction in pulmonary alveolar proteinosis".Orphanet Journal of Rare Diseases 11.1(2016):48.

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