|1.||Douillard-Guilloux, Gaëlle: 1 article (03/2010)|
|2.||Clave, Céline: 1 article (03/2010)|
|3.||Couraud, Pierre-Olivier: 1 article (03/2010)|
|4.||Miller, Florence: 1 article (03/2010)|
|5.||Caillaud, Catherine: 1 article (03/2010)|
|6.||Arfi, Audrey: 1 article (03/2010)|
|7.||Batista, Lionel: 1 article (03/2010)|
|1.||Sandhoff Disease (Sandhoff's Disease)
08/01/1990 - "Distribution and characterization of a Sandhoff disease-associated 50-kb deletion in the gene encoding the human beta-hexosaminidase beta-chain."
03/01/2010 - "Sandhoff disease is an autosomal recessive lysosomal disorder due to mutations in the beta-hexosaminidase beta-chain gene, resulting in beta-hexosaminidases A (alphabeta) and B (betabeta) deficiency and GM2 ganglioside accumulation in the brain. "
03/25/1989 - "Abnormal beta-hexosaminidase beta chain cDNA clones were isolated from a library constructed from cultured fibroblasts of a patient with a juvenile form of Sandhoff disease (genetic beta-hexosaminidase A and B deficiency). "
|1.||Complementary DNA (cDNA)
|3.||G(M2) Ganglioside (Ganglioside GM2)