載入...

Incomplete synthesis of N-glycans in congenital dyserythropoietic anemia type II caused by a defect in the gene encoding alpha-mannosidase II.

Congenital dyserythropoietic anemia type II, or hereditary erythroblastic multinuclearity with a positive acidified-serum-lysis test (HEMPAS), is a genetic anemia in humans inherited by an autosomally recessive mode. The enzyme defect in most HEMPAS patients has previously been proposed as a lowered...

全面介紹

Na minha lista:
書目詳細資料
Main Authors: Fukuda, M N, Masri, K A, Dell, A, Luzzatto, L, Moremen, K W
格式: Artigo
語言:Inglês
出版: 1990
主題:
在線閱讀:https://ncbi.nlm.nih.gov/pmc/articles/PMC54763/
https://ncbi.nlm.nih.gov/pubmed/2217175
標簽: 添加標簽
沒有標簽, 成為第一個標記此記錄!