文献
J-GLOBAL ID:202102225102713547
整理番号:21A0018784
FBLIM1遺伝子における遺伝的変異は典型的患者グループにおけるSAPHO症候群と慢性再発性多巣性骨髄炎に寄与しない【JST・京大機械翻訳】
Genetic variants in FBLIM1 gene do not contribute to SAPHO syndrome and chronic recurrent multifocal osteomyelitis in typical patient groups
著者 (9件):
Assmann Gunter
(Department of Internal Medicine I, Jose-Carreras Centrum for Immuno- and Gene Therapy, University of Saarland Medical School, Homburg, Germany)
,
Kohm Michaela
(Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany)
,
Schuster Volker
(Hospital for Children and Adolescents, University of Leipzig, Leipzig, Germany)
,
Behrens Frank
(Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany)
,
Mossner Rotraut
(Department of Dermatology, Georg-August-University Gottingen, Gottingen, Germany)
,
Magnolo Nina
(Department of Dermatology, University of Muenster, Muenster, Germany)
,
Oji Vinzenz
(Department of Dermatology, University of Muenster, Muenster, Germany)
,
Burkhardt Harald
(Division of Rheumatology and IME, Fraunhofer Institute, Branch for Translational Medicine and Pharmacology, Goethe University, Frankfurt am Main, Germany)
,
Hueffmeier Ulrike
(Institute of Human Genetics, University Hospital Erlangen, Friedrich-Alexander-Universitaet Erlangen-Nuernberg, Erlangen, Germany)
資料名:
BMC Medical Genetics (Web)
(BMC Medical Genetics (Web))
巻:
21
号:
1
ページ:
1-7
発行年:
2020年
JST資料番号:
U7307A
ISSN:
1471-2350
資料種別:
逐次刊行物 (A)
記事区分:
原著論文
発行国:
イギリス (GBR)
言語:
英語 (EN)