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Volumn 30, Issue C, 1996, Pages 299-310

Chapter 7 HEMPAS: A genetic disorder caused by a defect in N-linked oligosaccharide synthesis

Author keywords

mannosidase II; MH; carbohydrate deficiency glycoprotein syndrome; CDA; CDGS; congenital dyserythropoietic anemia; GnT II; HEMPAS; hereditary erythroblastic multinuclearity with positive acidified serum lysis test; N acetylglucosaminyltransferase II; SDS; sodium dodecyl sulfate

Indexed keywords


EID: 77956707700     PISSN: 01677306     EISSN: None     Source Type: Book Series    
DOI: 10.1016/S0167-7306(08)60293-8     Document Type: Article
Times cited : (2)

References (43)
  • 32
    • 0027283744 scopus 로고
    • Tanner M.J.A., and Anstee D.J. (Eds), W.B. Saunders Co., Philadelphia, PA.
    • Fukuda M.N. In: Tanner M.J.A., and Anstee D.J. (Eds). Bailliere's Clinical Haematology (1993), W.B. Saunders Co., Philadelphia, PA. 493-511
    • (1993) Bailliere's Clinical Haematology , pp. 493-511
    • Fukuda, M.N.1


* 이 정보는 Elsevier사의 SCOPUS DB에서 KISTI가 분석하여 추출한 것입니다.