Associated Papers
Genetic investigations on singleton school aged children reveal novel variants and new candidate genes for hearing loss.
Khan H et al.
Scientific Reports, 2024
39271758 (PubMed )
Supplement: 41598_2024_71407_MOESM1_ESM.xlsx › HPK7_het
Eukaryotic translation initiation factor 4-γ, 1 gene mutations are rare in Parkinson's disease among Taiwanese.
Weng YC et al.
Journal of the Formosan Medical Association = Taiwan Yi Zhi, 2016
The EIF4G1 gene and Parkinson's disease.
Deng H et al.
Acta Neurologica Scandinavica, 2015
Mutations in EIF4G1 are not a common cause of Parkinson's disease.
Siitonen A et al.
European Journal of Neurology, 2013
Study of the genetic variability in a Parkinson's Disease gene: EIF4G1.
Tucci A et al.
Neuroscience Letters, 2012
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