Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome

Niehues T, Oezguer TT, Bickes M, Waldmann R, Schoening J, Braesen J, Hagel C, Ballmaier M, Klusmann JH, Niedermayer A, Pannicke U, Enders A, Dueckers G, Siepermann K, Hempel J, Schwarz K, Viemann D (2020)

Publication Type: Journal article

Publication year: 2020

Journal

European Journal of Immunology Wiley-VCH Verlag

Book Volume: 50

Pages Range: 1078-1080

Journal Issue: 7

DOI: 10.1002/eji.201948504

Involved external institutions

Medizinische Hochschule Hannover (MHH) / Hannover Medical School DE Germany (DE) Universitätsklinikum Hamburg-Eppendorf (UKE) DE Germany (DE) Martin-Luther-Universität Halle-Wittenberg (MLU) DE Germany (DE) Universität Ulm DE Germany (DE) Australian National University (ANU) AU Australia (AU) HELIOS Kliniken DE Germany (DE)

How to cite

APA:

Niehues, T., Oezguer, T.T., Bickes, M., Waldmann, R., Schoening, J., Braesen, J.,... Viemann, D. (2020). Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome. European Journal of Immunology, 50(7), 1078-1080. https://doi.org/10.1002/eji.201948504

MLA:

Niehues, Tim, et al. "Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome." European Journal of Immunology 50.7 (2020): 1078-1080.

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