Bradley Neville Smith
King's College London
32 papers found
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ATXN2 Trinucleotide Repeat Length Correlates with Risk of ALS
Download from doi.orgNEK1 variants confer susceptibility to amyotrophic lateral sclerosis
Download from eprints.whiterose.ac.ukThe CHCHD10 P34S variant is not associated with ALS in a UK cohort of familial and sporadic patients
Download from hdl.handle.netNovel mutations support a role for Profilin 1 in the pathogenesis of ALS
Download from www.ncbi.nlm.nih.govVCP mutations are not a major cause of familial amyotrophic lateral sclerosis in the UK
Download from hdl.handle.netExome-wide Rare Variant Analysis Identifies TUBA4A Mutations Associated with Familial ALS.
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