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

Tim Niehues; Tuba Turul Özgür; Marie Bickes; Rebekka Waldmann; Jennifer Schöning; Jan Bräsen; Christian Hagel; Matthias Ballmaier; Jan Henning Klusmann; Alexandra Niedermayer; Ulrich Pannicke; Anselm Enders; Gregor Dückers; Kathrin Siepermann; Julyia Hempel; Klaus Schwarz; Dorothee Viemann

doi:10.1002/eji.201948504

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

Tim Niehues^*, Tuba Turul Özgür, Marie Bickes, Rebekka Waldmann, Jennifer Schöning, Jan Bräsen, Christian Hagel, Matthias Ballmaier, Jan Henning Klusmann, Alexandra Niedermayer, Ulrich Pannicke, Anselm Enders, Gregor Dückers, Kathrin Siepermann, Julyia Hempel, Klaus Schwarz, Dorothee Viemann

^*Corresponding author for this work

Research output: Contribution to journal › Letter › peer-review

20 Citations (Scopus)

Original language	English
Pages (from-to)	1078-1080
Number of pages	3
Journal	European Journal of Immunology
Volume	50
Issue number	7
DOIs	https://doi.org/10.1002/eji.201948504
Publication status	Published - 1 Jul 2020

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Niehues, T., Özgür, T. T., Bickes, M., Waldmann, R., Schöning, J., Bräsen, J., Hagel, C., Ballmaier, M., Klusmann, J. H., Niedermayer, A., Pannicke, U., Enders, A., Dückers, G., Siepermann, K., Hempel, J., Schwarz, K., & 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

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

keywords = "B cell development, cardiomyopathy, immunodeficiency, metabolism, myopathy",

author = "Tim Niehues and {\"O}zg{\"u}r, {Tuba Turul} and Marie Bickes and Rebekka Waldmann and Jennifer Sch{\"o}ning and Jan Br{\"a}sen and Christian Hagel and Matthias Ballmaier and Klusmann, {Jan Henning} and Alexandra Niedermayer and Ulrich Pannicke and Anselm Enders and Gregor D{\"u}ckers and Kathrin Siepermann and Julyia Hempel and Klaus Schwarz and Dorothee Viemann",

year = "2020",

month = jul,

day = "1",

doi = "10.1002/eji.201948504",

language = "English",

volume = "50",

pages = "1078--1080",

journal = "European Journal of Immunology",

issn = "0014-2980",

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Niehues, T, Özgür, TT, Bickes, M, Waldmann, R, Schöning, J, Bräsen, J, Hagel, C, Ballmaier, M, Klusmann, JH, Niedermayer, A, Pannicke, U, Enders, A, Dückers, G, Siepermann, K, Hempel, J, Schwarz, K & 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, vol. 50, no. 7, pp. 1078-1080. https://doi.org/10.1002/eji.201948504

TY - JOUR

T1 - Mutations of the gene FNIP1 associated with a syndromic autosomal recessive immunodeficiency with cardiomyopathy and pre-excitation syndrome

AU - Niehues, Tim

AU - Özgür, Tuba Turul

AU - Bickes, Marie

AU - Waldmann, Rebekka

AU - Schöning, Jennifer

AU - Bräsen, Jan

AU - Hagel, Christian

AU - Ballmaier, Matthias

AU - Klusmann, Jan Henning

AU - Niedermayer, Alexandra

AU - Pannicke, Ulrich

AU - Enders, Anselm

AU - Dückers, Gregor

AU - Siepermann, Kathrin

AU - Hempel, Julyia

AU - Schwarz, Klaus

AU - Viemann, Dorothee

PY - 2020/7/1

Y1 - 2020/7/1

KW - B cell development

KW - cardiomyopathy

KW - immunodeficiency

KW - metabolism

KW - myopathy

UR - http://www.scopus.com/inward/record.url?scp=85083649951&partnerID=8YFLogxK

U2 - 10.1002/eji.201948504

DO - 10.1002/eji.201948504

M3 - Letter

SN - 0014-2980

VL - 50

SP - 1078

EP - 1080

JO - European Journal of Immunology

JF - European Journal of Immunology

IS - 7

ER -

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

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