Kleine-Levin syndrome is associated with birth difficulties and genetic variants in the TRANK1 gene loci.
Ambati A, Hillary R, Leu-Semenescu S, Ollila HM, Lin L, During EH, Farber N, Rico TJ, Faraco J, Leary E, Goldstein-Piekarski AN, Huang YS, Han F, Sivan Y, Lecendreux M, Dodet P, Honda M, Gadoth N, Nevsimalova S, Pizza F, Kanbayashi T, Peraita-Adrados R, Leschziner GD, Hasan R, Canellas F, Kume K, Daniilidou M, Bourgin P, Rye D, Vicario JL, Hogl B, Hong SC, Plazzi G, Mayer G, Landtblom AM, Dauvilliers Y, Arnulf I, Mignot EJ.
Ambati A, et al.
Proc Natl Acad Sci U S A. 2021 Mar 23;118(12):e2005753118. doi: 10.1073/pnas.2005753118.
Proc Natl Acad Sci U S A. 2021.
PMID: 33737391
Free PMC article.
Kleine-Levin syndrome (KLS) is a rare disorder characterized by severe episodic hypersomnia, with cognitive impairment accompanied by apathy or disinhibition. ...While the rs71947865 association did not replicate in the entire follow-up sample of 171 KLS case …
Kleine-Levin syndrome (KLS) is a rare disorder characterized by severe episodic hypersomnia, with cognitive impairment …