Vincent Plagnol
University of Southern California
123 papers found
Refreshing results…
DYX1C1 is required for axonemal dynein assembly and ciliary motility
Download from europepmc.orgNegligible impact of rare autoimmune-locus coding-region variants on missing heritability
Download from www.nature.comCNV Analysis in Tourette Syndrome Implicates Large Genomic Rearrangements in COL8A1 and NRXN1
Download from dx.doi.orgConstitutional Mutations in RTEL1 Cause Severe Dyskeratosis Congenita
Download from www.ncbi.nlm.nih.govISPD gene mutations are a common cause of congenital and limb-girdle muscular dystrophies.
Download from discovery.ucl.ac.ukMutations in ANO3 Cause Dominant Craniocervical Dystonia: Ion Channel Implicated in Pathogenesis
Download from www.ncbi.nlm.nih.govLRBA gene deletion in a patient presenting with autoimmunity without hypogammaglobulinemia
Download from europepmc.orgKohlschütter–Tönz Syndrome: Mutations in ROGDI and Evidence of Genetic Heterogeneity
Download from www.ncbi.nlm.nih.govMissing publications? Search for publications with a matching author name.