학술논문

Integrin-a3 mutations with kidney, lung, and skin disease

Document Type

Case study

Author

Has, Cristina; Sparta, Giuseppina; Kiritsi, Dimitra; Weibel, Lisa; Moeller, Alexander; Vega-Warner, Virginia; Waters, Aoife; Yinghong He; Anikster, Yair; Esser, Philipp; Straub, Beate K.; Hausser, Ingrid; Bockenhauer, Detlef; Dekel, Benjamin; Hildebrandt, Friedhelm; Bruckner-Tuderman, Leena; Laube, Guido F.

Source

The New England Journal of Medicine. April 19, 2012, Vol. 366 Issue 16, p1508, 7 p.

Subject

Research
Causes of
Genetic aspects
Case studies
Health aspects
Cell interactions -- Research
Comorbidity -- Causes of
Comorbidity -- Genetic aspects
Comorbidity -- Case studies
Gene mutation -- Research
Integrins -- Research
Integrins -- Health aspects
Interstitial lung diseases -- Causes of
Interstitial lung diseases -- Genetic aspects
Nephrotic syndrome -- Causes of
Nephrotic syndrome -- Genetic aspects
Skin aging -- Genetic aspects
Cell interaction -- Research
Gene mutations -- Research
Lung diseases, Interstitial -- Causes of
Lung diseases, Interstitial -- Genetic aspects
Skin -- Aging
Skin -- Genetic aspects

Language

English

ISSN

0028-4793

Abstract

The article discusses the association of integrin-[alpha]3 transmembrane integrin receptor (ITAG3) mutations with kidney, lung, and skin disease. The cases of 3 patients are highlighted to arrive at a better understanding of ITAG3 mutations and how indispensible it is.

Online Access

Full Text(NEJM) Full Text (ProQuest Central) Web of Science JCR 저널정보 Scopus Find it@PNU

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