APA

Traoré M., Landouré G., Motley W., Sangaré M., Meilleur K., Coulibaly S., Traoré S., Niaré B., Mochel F., La Pean A., Vortmeyer A., Mani H. & Fischbeck K. H. (20091207). Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. : Neurogenetics.

Chicago

Traoré M, Landouré G, Motley W, Sangaré M, Meilleur K, Coulibaly S, Traoré S, Niaré B, Mochel F, La Pean A, Vortmeyer A, Mani H and Fischbeck K H. 20091207. Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. : Neurogenetics.

Harvard

Traoré M., Landouré G., Motley W., Sangaré M., Meilleur K., Coulibaly S., Traoré S., Niaré B., Mochel F., La Pean A., Vortmeyer A., Mani H. and Fischbeck K. H. (20091207). Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. : Neurogenetics.

MLA

Traoré M, Landouré G, Motley W, Sangaré M, Meilleur K, Coulibaly S, Traoré S, Niaré B, Mochel F, La Pean A, Vortmeyer A, Mani H and Fischbeck K H. Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease. : Neurogenetics. 20091207.