A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy.
about
Missense mutations in TENM4, a regulator of axon guidance and central myelination, cause essential tremorSleep, plasticity and the pathophysiology of neurodevelopmental disorders: the potential roles of protein synthesis and other cellular processes.Circadian Rhythms, Sleep, and Disorders of AgingComorbidity of Narcolepsy Type 1 With Autoimmune Diseases and Other Immunopathological Disorders: A Case-Control Study.A statistical framework to guide sequencing choices in pedigrees.The European Narcolepsy Network (EU-NN) database.Narcolepsy Type 1 as an Autoimmune Disorder: Evidence, and Implications for Pharmacological Treatment.HLA DQB1*06:02 negative narcolepsy with hypocretin/orexin deficiency.DNA methyltransferase 1 mutations and mitochondrial pathology: is mtDNA methylated?Narcolepsy with cataplexy and comorbid immunopathological diseases.Narcolepsy is a common phenotype in HSAN IE and ADCA-DN.
P2860
Q28118169-E56B7585-29E1-42CE-A864-301257CFD9FAQ30823493-6DB03230-84EC-4164-A7AA-A7235BE3A46EQ36731044-010F009A-B7EC-41C2-B798-C72C67F0CA82Q36971646-7890E724-55B9-4346-8F6B-CB08D93D68A5Q37592304-69A9E300-AA99-4F28-B6F7-58481CC45B11Q40062905-3BF5B2B0-FDA8-4E79-BE58-BEE0C66472C7Q41995022-9F9511D8-A63D-4F56-84C0-FE85002F5C57Q42913561-0D259EDB-9C2E-4106-AC99-DEC0A7B27A8DQ43184131-A199D6C9-7A74-46B0-BB62-75DFB7206C7BQ43622431-273E8CEC-C392-4794-8313-8866CEC0CFAAQ48113682-8341314B-D1C5-485E-A27E-D2CF8ECC2217
P2860
A missense mutation in myelin oligodendrocyte glycoprotein as a cause of familial narcolepsy with cataplexy.
description
2011 nî lūn-bûn
@nan
2011 թուականի Սեպտեմբերին հրատարակուած գիտական յօդուած
@hyw
2011 թվականի սեպտեմբերին հրատարակված գիտական հոդված
@hy
2011年の論文
@ja
2011年論文
@yue
2011年論文
@zh-hant
2011年論文
@zh-hk
2011年論文
@zh-mo
2011年論文
@zh-tw
2011年论文
@wuu
name
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@ast
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@en
type
label
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@ast
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@en
prefLabel
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@ast
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@en
P2093
P2860
P50
P1476
A missense mutation in myelin ...... ial narcolepsy with cataplexy.
@en
P2093
Clara de Andrés
Corinne Pfister
Gert J Lammers
José L Vicário
Luca Bartesaghi
Nicolas Guex
Rosa Peraita-Adrados
P2860
P304
P356
10.1016/J.AJHG.2011.08.007
P407
P577
2011-09-01T00:00:00Z