PUBLICATION
CORRECTION: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome
- Authors
- Luo, M., Lin, Z., Zhu, T., Jin, M., Meng, D., He, R., Cao, Z., Shen, Y., Lu, C., Cai, R., Zhao, Y., Wang, X., Li, H., Wu, S., Zou, X., Luo, G., Cao, L., Huang, M., Jiao, H., Gao, H., Sui, R., Zhao, C., Ma, X., Cao, M.
- ID
- ZDB-PUB-220906-240
- Date
- 2021
- Source
- Genetics in medicine : official journal of the American College of Medical Genetics 23: 1175 (Other)
- Registered Authors
- Keywords
- none
- MeSH Terms
- none
- PubMed
- 33972723 Full text @ Genet. Med.
Citation
Luo, M., Lin, Z., Zhu, T., Jin, M., Meng, D., He, R., Cao, Z., Shen, Y., Lu, C., Cai, R., Zhao, Y., Wang, X., Li, H., Wu, S., Zou, X., Luo, G., Cao, L., Huang, M., Jiao, H., Gao, H., Sui, R., Zhao, C., Ma, X., Cao, M. (2021) CORRECTION: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome. Genetics in medicine : official journal of the American College of Medical Genetics. 23:1175.
Abstract
The original article can be found online at https://doi.org/10.1038/s41436-021-01106-z.
Correction to: Genetics in Medicine 2021; https://doi.org/10.1038/s41436-021-01106-z; published online 02 February 2021
Due to a processing error, the online graphical abstract was not given.
Errata / Notes
This article corrects ZDB-PUB-210204-5 .
Genes / Markers
Expression
Phenotype
Mutations / Transgenics
Human Disease / Model
Sequence Targeting Reagents
Fish
Orthology
Engineered Foreign Genes
Mapping