A novel C1 inhibitor gene mutation in a family with hereditary angioedema: Use of genetic analysis to facilitate early diagnosis

Affiliations

¹ Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan. Electronic address: kojiy@kuhp.kyoto-u.ac.jp.
² Department of Internal Medicine, Kyusyu University Beppu Hospital, Oita, Japan; Center for Research, Education, and Treatment of AngioEdema (CREATE), A Specified Non-profit Corporation, Fukuoka, Japan.
³ Center for Research, Education, and Treatment of AngioEdema (CREATE), A Specified Non-profit Corporation, Fukuoka, Japan; Department of Clinical Research, National Kyushu Medical Center, Fukuoka, Japan.
⁴ Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.

Free article

Case Reports

Koji Yokoyama et al. Allergol Int. 2020 Jan.

Free article

. 2020 Jan;69(1):148-149.

doi: 10.1016/j.alit.2019.07.005. Epub 2019 Aug 10.

¹ Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan. Electronic address: kojiy@kuhp.kyoto-u.ac.jp.
² Department of Internal Medicine, Kyusyu University Beppu Hospital, Oita, Japan; Center for Research, Education, and Treatment of AngioEdema (CREATE), A Specified Non-profit Corporation, Fukuoka, Japan.
³ Center for Research, Education, and Treatment of AngioEdema (CREATE), A Specified Non-profit Corporation, Fukuoka, Japan; Department of Clinical Research, National Kyushu Medical Center, Fukuoka, Japan.
⁴ Department of Pediatrics, Japanese Red Cross Wakayama Medical Center, Wakayama, Japan.

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