Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.
about
New Genes Causing Hereditary Parkinson's Disease or Parkinsonism.Adenosine A1-A2A Receptor Heteromer as a Possible Target for Early-Onset Parkinson's Disease.Targeting Adenosine Signaling in Parkinson's Disease: From Pharmacological to Non-pharmacological Approaches.ADORA1 mutations are not a common cause of Parkinson's disease and dementia with Lewy bodies.PTRHD1 (C2orf79) mutations lead to autosomal-recessive intellectual disability and parkinsonism.Biochemical and Pharmacological Role of A1 Adenosine Receptors and Their Modulation as Novel Therapeutic Strategy.PTRHD1 and possibly ADORA1 mutations contribute to Parkinsonism with intellectual disability.
P2860
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P2860
Mutation in ADORA1 identified as likely cause of early-onset parkinsonism and cognitive dysfunction.
description
2016 nî lūn-bûn
@nan
2016 թուականի Մայիսին հրատարակուած գիտական յօդուած
@hyw
2016 թվականի մայիսին հրատարակված գիտական հոդված
@hy
2016年の論文
@ja
2016年論文
@yue
2016年論文
@zh-hant
2016年論文
@zh-hk
2016年論文
@zh-mo
2016年論文
@zh-tw
2016年论文
@wuu
name
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@ast
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@en
type
label
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@ast
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@en
prefLabel
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@ast
Mutation in ADORA1 identified ...... ism and cognitive dysfunction.
@en
P2093
P2860
P356
P1433
P1476
Mutation in ADORA1 identified ...... nism and cognitive dysfunction
@en
P2093
Abolfazl Moghadam
Brandy Klotzle
Casey Turk
Ehsan Arefian
Elahe Elahi
Elham Jaberi
Farid Keramatian
Frank Steemers
Gholam Ali Shahidi
Jian-Bing Fan
P2860
P304
P356
10.1002/MDS.26627
P407
P577
2016-05-02T00:00:00Z