Associated Papers
In vivo validation of late-onset Alzheimer's disease genetic risk factors.
Sasner M et al.
Alzheimer's & Dementia : the Journal of the Alzheimer's Association, 2024
In vivo validation of late-onset Alzheimer's disease genetic risk factors.
Sasner M et al.
Biorxiv : the Preprint Server for Biology, 2023
Novel compound heterozygous MYO7A mutations in Moroccan families with autosomal recessive non-syndromic hearing loss.
Bakhchane A et al.
Plos One, 2017
28472130 (PubMed )
Supplement: pone.0176516.s002.xlsx › Feuil1
The eSNV-detect: a computational system to identify expressed single nucleotide variants from transcriptome sequencing data.
Tang X et al.
Nucleic Acids Research, 2014
25352556 (PubMed )
Supplement: supp_gku1005_nar-01266-met-n-2014-File012.xlsx › TCGA-A2-A0ER-01A.domain
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