MeCP2 mutations: progress towards understanding and treating Rett syndrome
about
Persistent Unresolved Inflammation in the Mecp2-308 Female Mutated Mouse Model of Rett SyndromeDevelopment of the Tailored Rett Intervention and Assessment Longitudinal (TRIAL) database and the Rett Evaluation of Symptoms and Treatments (REST) Questionnaire.Role of MeCP2 in neurological disorders: current status and future perspectives.
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MeCP2 mutations: progress towards understanding and treating Rett syndrome
description
2017 nî lūn-bûn
@nan
2017年の論文
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2017年論文
@yue
2017年論文
@zh-hant
2017年論文
@zh-hk
2017年論文
@zh-mo
2017年論文
@zh-tw
2017年论文
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2017年论文
@zh
2017年论文
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name
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@en
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@nl
type
label
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@en
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@nl
prefLabel
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@en
MeCP2 mutations: progress towards understanding and treating Rett syndrome
@nl
P2860
P31
P921
P1433
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MeCP2 mutations: progress towards understanding and treating Rett syndrome
@en
P2860
P2888
P356
10.1186/S13073-017-0411-7
P5008
P577
2017-02-17T00:00:00Z
P6179
1083847192