Genomic mutations associated with mild and severe deficiencies of transcobalamin I (haptocorrin) that cause mildly and severely low serum cobalamin levels

标题
Genomic mutations associated with mild and severe deficiencies of transcobalamin I (haptocorrin) that cause mildly and severely low serum cobalamin levels
作者
关键词
-
出版物
BRITISH JOURNAL OF HAEMATOLOGY
Volume 147, Issue 3, Pages 386-391
出版商
Wiley
发表日期
2009-08-18
DOI
10.1111/j.1365-2141.2009.07855.x

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