Items where authors include "Leo, V."

Article

Johnson, B., Lowe, G.C., Futterer, J. et al. (31 more authors) (2016) Whole exome sequencing identifies genetic variants in inherited thrombocytopenia with secondary qualitative function defects. Haematologica. ISSN 0390-6078

Ashrafian, H., Docherty, L., Leo, V. et al. (22 more authors) (2010) A Mutation in the Mitochondrial Fission Gene Dnm1l Leads to Cardiomyopathy. PLoS Genetics, 6 (6). e1001000. ISSN 1553-7390

Carpenter, D., Ringrose, C., Leo, V. et al. (5 more authors) (2009) The role of CACNA1S in predisposition to malignant hyperthermia. BMC Medical Genetics , 10. ISSN 1471-2350