Bradley Neville Smith
King's College London
32 papers found
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H63D polymorphism in HFE is not associated with amyotrophic lateral sclerosis
Download from lirias.kuleuven.beThe C9ORF72 expansion mutation is a common cause of ALS+/−FTD in Europe and has a single founder
Download from www.nature.comFamilial amyotrophic lateral sclerosis is associated with a mutation in D-amino acid oxidase
Download from doi.orgMutations in FUS, an RNA Processing Protein, Cause Familial Amyotrophic Lateral Sclerosis Type 6
Download from www.ncbi.nlm.nih.govHair analysis for drugs: technological breakthrough or ethical quagmire?
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