Associated Papers
Identification of heritable rare variants associated with early-stage lung adenocarcinoma risk.
Fu R et al.
Translational Lung Cancer Research, 2022
35529798 (PubMed )
Supplement: tlcr-11-04-509-supplementary.pdf
VPOT: A Customizable Variant Prioritization Ordering Tool for Annotated Variants.
Ip E et al.
Genomics, Proteomics & Bioinformatics, 2019
Mutations in riboflavin transporter present with severe sensory loss and deafness in childhood.
Srour M et al.
Muscle & Nerve, 2014
Exome sequencing reveals riboflavin transporter mutations as a cause of motor neuron disease.
Johnson JO et al.
Brain : a Journal of Neurology, 2012
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