Exome sequencing analysis reveals two novel mutations in TTC37 in Chinese patients with Crohn's disease
QJM
.
2024 Feb 26;117(2):145-147.
doi: 10.1093/qjmed/hcad243.
Authors
Y Zhang
1
2
3
,
X Yang
1
2
3
,
S Guo
4
,
L Tao
1
2
3
,
R Xiang
2
4
,
H Huang
2
4
,
H Yang
1
2
3
Affiliations
1
Department of Gastroenterology, Xiangya Hospital, Central South University, Changsha, China.
2
Hunan Key Laboratory of Organ Fibrosis, Central South University, Changsha, China.
3
National Clinical Research Center for Geriatric Disorders, Xiangya Hospital, Central South University, Changsha, China.
4
Department of Cell Biology, School of Life Science, Central South University, Changsha, China.
PMID:
37878822
DOI:
10.1093/qjmed/hcad243
No abstract available
MeSH terms
Carrier Proteins / genetics
China
Crohn Disease* / genetics
Exome Sequencing
Genetic Testing
Humans
Mutation
Substances
TTC37 protein, human
Carrier Proteins
Grants and funding
81873585/Natural Science Foundation of China
2020TQ0363/China Postdoctoral Science Foundation
2021JJ40992/Natural Science Foundation of Hunan Province
2021Q11/Youth Science Foundation of Xiangya Hospital