Mutations in the TSPAN12 and KIF11 Genes in Severe Retinopathy of Prematurity
Indian J Pediatr
.
2023 Apr;90(4):408.
doi: 10.1007/s12098-023-04504-0.
Epub 2023 Feb 11.
Authors
Huiqing Sun
1
,
Zhiyi Xia
2
,
Zhansheng Wang
3
,
Lifeng Li
4
,
Yuebing Lu
5
,
Li Li
6
,
Lei Liu
2
,
Jing Liu
2
Affiliations
1
Department of Neonatology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, 33 Longhuwaihuan Road, Zhengzhou, 450018, China. s_huiqing@sina.com.
2
Key Laboratories of Children's Genetic Metabolic Diseases, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou, Henan Province, China.
3
Department of Neonatology, Shangqiu People's Hospital, Shangqiu, Henan Province, China.
4
Department of Neonatology, Children's Hospital Affiliated to Zhengzhou University, Henan Children's Hospital, Zhengzhou Children's Hospital, 33 Longhuwaihuan Road, Zhengzhou, 450018, China.
5
Department of Ophthalmology, Children's Hospital Affiliated to Zhengzhou University, 33 Longhuwaihuan Road, Zhengzhou, 450018, China.
6
Department of Neonatology, Luoyang Maternal and Children's Hospital, Luoyang, Henan Province, China.
PMID:
36773199
DOI:
10.1007/s12098-023-04504-0
No abstract available
Publication types
Letter
MeSH terms
Humans
Infant, Newborn
Infant, Premature
Kinesins / genetics
Mutation
Retinopathy of Prematurity* / genetics
Tetraspanins / genetics
Substances
KIF11 protein, human
Kinesins
TSPAN12 protein, human
Tetraspanins
Grants and funding
162102310001/Department of Science and Technology of Henan Province of China