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학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
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연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2018.1
- 수록면
- 185 - 188 (4page)
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Dear Editor, Congenital analbuminemia (CAA; OMIM # 616000) is a rare autosomal recessive disorder characterized by the complete absence (or extremely low level) of serum albumin (ALB), and is usually diagnosed by serum protein electrophoresis [1]. Since different clinical conditions can result in hypoalbuminemia, mutation analysis of ALB gene is always necessary to confirm the diagnosis of CAA. Since the low ALB level is partially compensated by an increase of other serum proteins
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등록된 정보가 없습니다.
참고문헌 (8)
참고문헌 신청
Peters T Jr / 1996 / All about albumin: biochemistry, genetics and medical Applications / Academic Press :1~432
Minchiotti L / 2013 / Congenital analbuminaemia: Molecular defects and biochemical and clinical aspects / Biochim Biophys Acta 1830:5494~5502
The Albumin Website
Watkins S / 1994 / A nucleotide insertion and frameshift cause analbuminemia in an Italian family / Proc Natl Acad Sci USA 91:2275~2279
Toye JM / 2012 / Perinatal and childhood morbidity and mortality in congenital analbuminemia / Paediatr Child Health 17:20~23
Minchiotti L / 2013 / Congenital analbuminaemia: Molecular defects and biochemical and clinical aspects / Biochim Biophys Acta 1830:5494~5502
The Albumin Website
Watkins S / 1994 / A nucleotide insertion and frameshift cause analbuminemia in an Italian family / Proc Natl Acad Sci USA 91:2275~2279
Toye JM / 2012 / Perinatal and childhood morbidity and mortality in congenital analbuminemia / Paediatr Child Health 17:20~23
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