Summary statistics are available for download from the authors.
Publications
Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci.
Ambati A, et al.
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12):e2005753118. doi:10.1073/pnas.2005753118.
PMID: 33737391
Phenotypes
- Kleine-Levin syndrome
Experiment summary
This study analyzed genetic associations for Kleine-Levin syndrome (KLS), a rare disorder characterized by severe episodic hypersomnia, with cognitive impairment accompanied by apathy or disinhibition, in 673 KLS cases and 15,341 ethnically matched control individuals.
Dataset ID
Ambati2021_KleineLevinSynd_Mixed