受强制性开放获取政策约束的文章 - Sadeq Vallian, MSc, PhD了解详情
无法在其他位置公开访问的文章：3 篇
F1174V mutation alters the ALK active conformation in response to Crizotinib in NSCLC: Insight from molecular simulations
F Dehghanian, M Kay, S Vallian
Journal of Molecular Graphics and Modelling 75, 287-293, 2017
强制性开放获取政策： US National Institutes of Health
Association of rs1738074 polymorphism of TAGAP gene with susceptibility to multiple sclerosis in the Iranian population
A Jazaeri, S Vallian
Neuroscience Letters 648, 66-69, 2017
强制性开放获取政策： US National Institutes of Health
AOPEP variants as a novel cause of recessive dystonia: Generalized dystonia and dystonia-parkinsonism
B Garavaglia, S Vallian, LM Romito, G Straccia, M Capecci, F Invernizzi, ...
Parkinsonism & Related Disorders 97, 52-56, 2022
强制性开放获取政策： German Research Foundation, Helmholtz Association
可在其他位置公开访问的文章：2 篇
SCUBE3 loss-of-function causes a recognizable recessive developmental disorder due to defective bone morphogenetic protein signaling
YC Lin, M Niceta, V Muto, B Vona, AT Pagnamenta, R Maroofian, C Beetz, ...
The American Journal of Human Genetics 108 (1), 115-133, 2021
强制性开放获取政策： Department of Science & Technology, India, National Institute for Health …
Mutations in EPG5 are associated with a wide spectrum of neurodevelopmental and neurodegenerative disorders
HS Dafsari, C Deneubourg, K Singh, R Maroofian, Z Suprenant, AL Kho, ...
medRxiv, 2024.06. 12.24308722, 2024
强制性开放获取政策： Netherlands Organisation for Scientific Research, European Commission …
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