Bi-allelic variants in HCRT cause autosomal recessive narcolepsy
Author:
Publisher
Springer Science and Business Media LLC
Subject
Cellular and Molecular Neuroscience,Genetics (clinical),Genetics
Link
https://link.springer.com/content/pdf/10.1007/s10048-024-00744-0.pdf
Reference11 articles.
1. Barateau L, Pizza F, Plazzi G, Dauvilliers Y (2022) Narcolepsy. J Sleep Res 31:e13631
2. Ollila HM, Sharon E, Lin L, Sinnott-Armstrong N, Ambati A, Yogeshwar SM et al (2023) Narcolepsy risk loci outline role of T cell autoimmunity and infectious triggers in narcolepsy. Nat Commun 14:2709
3. Peyron C, Faraco J, Rogers W, Ripley B, Overeem S, Charnay Y et al (2000) A mutation in a case of early onset narcolepsy and a generalized absence of hypocretin peptides in human narcoleptic brains. Nat Med 6:991–997
4. Degn M, Dauvilliers Y, Dreisig K, Lopez R, Pfister C, Pradervand S et al (2017) Rare missense mutations in P2RY11 in narcolepsy with cataplexy. Brain 140:1657–1668
5. Liblau RS, Vassalli A, Seifinejad A, Tafti M (2015) Hypocretin (orexin) biology and the pathophysiology of narcolepsy with cataplexy. Lancet Neurol 14:318–328
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