지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2024.1
- 수록면
- 123 - 126 (4page)
- DOI
- https://doi.org/10.14802/jmd.23188
이용수
초록· 키워드
오류제보하기
Wilson’s disease (WD) is an autosomal recessive disorder of copper metabolism caused by mutations in the ATP7B gene. Pathogenic variants can lead to defects in or a loss of function of the P-type ATPase facilitating copper transport, resulting in a biliary copper excretion disorder.
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