Mutations in HTRA2 are not a common cause of familial classic ET.
about
Knowledge gaps and research recommendations for essential tremor.A step toward essential tremor gene discovery: identification of extreme phenotype and screening of HTRA2 and ANO3Mutation Analysis of HTRA2 Gene in Chinese Familial Essential Tremor and Familial Parkinson's Disease.Cerebellar Pathology in Familial vs. Sporadic Essential Tremor.Climbing fiber-Purkinje cell synaptic pathology across essential tremor subtypes.
P2860
Mutations in HTRA2 are not a common cause of familial classic ET.
description
2015 nî lūn-bûn
@nan
2015年の論文
@ja
2015年学术文章
@wuu
2015年学术文章
@zh
2015年学术文章
@zh-cn
2015年学术文章
@zh-hans
2015年学术文章
@zh-my
2015年学术文章
@zh-sg
2015年學術文章
@yue
2015年學術文章
@zh-hant
name
Mutations in HTRA2 are not a common cause of familial classic ET.
@en
Mutations in HTRA2 are not a common cause of familial classic ET.
@nl
type
label
Mutations in HTRA2 are not a common cause of familial classic ET.
@en
Mutations in HTRA2 are not a common cause of familial classic ET.
@nl
prefLabel
Mutations in HTRA2 are not a common cause of familial classic ET.
@en
Mutations in HTRA2 are not a common cause of familial classic ET.
@nl
P2093
P2860
P50
P356
P1433
P1476
Mutations in HTRA2 are not a common cause of familial classic ET
@en
P2093
Delia Lorenz
Gregor Kuhlenbäumer
Stephan Klebe
P2860
P304
P356
10.1002/MDS.26252
P407
P577
2015-05-13T00:00:00Z