Jean Muller
Laboratoire de Génétique Médicale (UMR_S Inserm U1112)
43 papers found
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The Data Use Ontology to streamline responsible access to human biomedical datasets
Download from doi.orgNovel TTLL5 Variants Associated with Cone-Rod Dystrophy and Early-Onset Severe Retinal Dystrophy
Download from doi.orgGenes for spinocerebellar ataxia with blindness and deafness (SCABD/SCAR3, MIM# 271250 and SCABD2)
Download from www.nature.comKD4v: comprehensible knowledge discovery system for missense variant
Download from doi.orgNext generation sequencing for molecular diagnosis of neuromuscular diseases
Download from link.springer.comIdentifying single copy orthologs in Metazoa.
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