Clinical characteristics and genotype-phenotype correlations in C3 deficiency - 05/02/16
Doi : 10.1016/j.jaci.2015.08.017
Yuka Okura, MD, PhD a, b 
, Ichiro Kobayashi, MD, PhD a, Masafumi Yamada, MD, PhD a, Satoshi Sasaki, MD, PhD a, c, Yutaka Yamada, MD c, Ichiro Kamioka, MD, PhD d, Rie Kanai, MD, PhD e, Yutaka Takahashi, MD, PhD b, Tadashi Ariga, MD, PhD a
, Ichiro Kobayashi, MD, PhD a, Masafumi Yamada, MD, PhD a, Satoshi Sasaki, MD, PhD a, c, Yutaka Yamada, MD c, Ichiro Kamioka, MD, PhD d, Rie Kanai, MD, PhD e, Yutaka Takahashi, MD, PhD b, Tadashi Ariga, MD, PhD a a Department of Pediatrics, Hokkaido University Graduate School of Medicine, Sapporo, Japan
b Department of Pediatrics, KKR Sapporo Medical Center, Sapporo, Japan
c Department of Pediatrics, Hakodate Central General Hospital, Hakodate, Japan
d Department of Pediatrics, Kakogawa West City Hospital, Kakogawa, Japan
e Department of Pediatrics, Shimane University Faculty of Medicine, Izumo, Japan
| This work was supported in part by a grant for Research on Intractable Diseases from the Japanese Ministry of Health, Labor and Welfare. |
|
| Disclosure of potential conflict of interest: The authors declare that they have no relevant conflicts of interest. |
© 2015
American Academy of Allergy, Asthma & Immunology. Publié par Elsevier Masson SAS. Tous droits réservés.
Vol 137 - N° 2
P. 640 - février 2016 Retour au numéro
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