A case report of congenital erythropoietic anemia II in China with a novel mutation
Ann Hematol
.
2019 Apr;98(4):1041-1043.
doi: 10.1007/s00277-019-03612-2.
Epub 2019 Feb 12.
Authors
Hong Zhang
1
,
Wuqing Wan
2
,
Xiaoyan Liu
1
,
Chuan Wen
1
,
Ying Liu
1
,
Senlin Luo
1
,
Xiao Sun
1
,
Shizhe Liu
1
Affiliations
1
Department of Pediatrics, the Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China.
2
Department of Pediatrics, the Second Xiangya Hospital, Central South University, Changsha, 410011, Hunan, China. wanwuqing@csu.edu.cn.
PMID:
30747246
PMCID:
PMC6423316
DOI:
10.1007/s00277-019-03612-2
No abstract available
Publication types
Case Reports
Letter
MeSH terms
Anemia, Dyserythropoietic, Congenital / genetics*
Asian People
Child
China
Female
Humans
Mutation*
Vesicular Transport Proteins / genetics*
Substances
SEC23B protein, human
Vesicular Transport Proteins