Novel mutation in the NHLRC1 gene in a Malian family with a severe phenotype of Lafora disease.
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 KH.
Traoré M, et al. Among authors: coulibaly s.
Neurogenetics. 2009 Oct;10(4):319-23. doi: 10.1007/s10048-009-0190-4. Epub 2009 Mar 26.
Neurogenetics. 2009.
PMID: 19322595
Free PMC article.