alpha-synuclein and verified mutations in the protein - Biology bibliographies - in Harvard style

In-text: (Appel-Cresswell et al., 2013)

Your Bibliography: Appel-Cresswell, S., Vilarino-Guell, C., Encarnacion, M., Sherman, H., Yu, I., Shah, B., Weir, D., Thompson, C., Szu-Tu, C., Trinh, J., Aasly, J., Rajput, A., Rajput, A., Jon Stoessl, A. and Farrer, M., 2013. Alpha-synuclein p.H50Q, a novel pathogenic mutation for Parkinson's disease. Movement Disorders, 28(6), pp.811-813.

In-text: (Krüger et al., 1998)

Your Bibliography: Krüger, R., Kuhn, W., Müller, T., Woitalla, D., Graeber, M., Kösel, S., Przuntek, H., Epplen, J., Schols, L. and Riess, O., 1998. AlaSOPro mutation in the gene encoding α-synuclein in Parkinson's disease. Nat Genet, 18(2), pp.106-108.

In-text: (Lesage et al., 2013)

Your Bibliography: Lesage, S., Anheim, M., Letournel, F., Bousset, L., Honoré, A., Rozas, N., Pieri, L., Madiona, K., Dürr, A., Melki, R., Verny, C. and Brice, A., 2013. G51D α-synuclein mutation causes a novel Parkinsonian-pyramidal syndrome. Annals of Neurology, 73(4), pp.459-471.

In-text: (Pasanen et al., 2014)

Your Bibliography: Pasanen, P., Myllykangas, L., Siitonen, M., Raunio, A., Kaakkola, S., Lyytinen, J., Tienari, P., Pöyhönen, M. and Paetau, A., 2014. A novel α-synuclein mutation A53E associated with atypical multiple system atrophy and Parkinson's disease-type pathology. Neurobiology of Aging, 35(9), pp.2180.e1-2180.e5.

In-text: (Polymeropoulos et al., 1997)

Your Bibliography: Polymeropoulos, M., Lavedan, C., Leroy, E., Ide, S., Dehejia, A., Dutra, A., Pike, B., Root, H., Rubenstein, J., Boyer, R., Stenroos, E., Chandrasekharappa, S., Anthanassiadou, A., Papapetropoulos, T., Johnson, W., Lazzarini, A., Duvoisin, R., Di Iorio, G., Golbe, L. and Nussbaum, R., 1997. Mutation in the -Synuclein Gene Identified in Families with Parkinson's Disease. Science, 276(5321), pp.2045-2047.

In-text: (Zarranz et al., 2004)

Your Bibliography: Zarranz, J., Alegre, J., Gomez-Esteban, J., Lezcano, E., Ros, R., Ampuero, I., Vidal, L., Hoenicka, J., Rodriguez, O., Atares, B., Llorens, V., Tortosa, E., del Ser, T., Munoz, D. and de Yebenes, J., 2004. The new mutation, E46K, of ?-synuclein causes parkinson and Lewy body dementia. Annals of Neurology, 55(2), pp.164-173.