[Hereditary stomatocytosis with PIEZO1 gene mutations: report of five cases and literature review]
Zhonghua Xue Ye Xue Za Zhi
.
2019 Jun 14;40(6):518-521.
doi: 10.3760/cma.j.issn.0253-2727.2019.06.013.
[Article in Chinese]
Authors
Y Li
1
,
X Zhao
1
,
J P Li
1
,
Y H Xia
2
,
Y Li
1
,
W R Yang
1
,
L Ye
1
,
G X Peng
1
,
X B Han
3
,
Y H Li
4
,
H H Fan
1
,
L Song
1
,
Y Yang
1
,
K Zhou
1
,
Y Z Xiong
1
,
Q Y Wu
1
,
Z J Jing
1
,
L P Zhang
1
,
L Zhang
1
Affiliations
1
Therapeutic Center of Anemia, Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
2
Clinical Laboratory Center, Institute of Hematology and Blood Diseases Hospital, CAMS & PUMC, Tianjin 300020, China.
3
Hematology Department, Qian'an People's Hospital, Qian'an 064400, China.
4
Clinical Laboratory, Qian'an People's Hospital, Qian'an 064400, China.
PMID:
31340627
PMCID:
PMC7342391
DOI:
10.3760/cma.j.issn.0253-2727.2019.06.013
No abstract available
Publication types
Case Reports
Review
MeSH terms
Anemia, Hemolytic, Congenital*
Humans
Ion Channels / genetics*
Mutation
Substances
Ion Channels
PIEZO1 protein, human
Grants and funding
基金项目:国家科技重大专项课题(2017ZX09304024);天津市血液病临床医学研究中心建设项目(15ZXLCSY00010)