CC: CCSD:49455
AU: Navon R; Khosravi R; Korczyn T; Masson M; Sonnino S; Fardeau M;
    Eymard B; Lefevre M; Turpin JC; Rondot P; Baumann N
TI: A new mutation in the HEXA gene associated with a spinal muscular
    atrophy phenotype
CT: Neurology (1995) 45: 539-543 [PMID:7898712]
BS: (CN) human, (OT) gangliosidosis
TN: GM2
MT: ganglioside
MT: glycolipid
MT: glycosphingolipid
SB: Westra B
DA: 30-04-1996
FC: f7673cea
SI: CBank:16359
----------------
structure:

 b-D-GalpNAc-(1-4)+
                  |
             b-D-Galp-(1-4)-b-D-Glcp-(1-1)-Ceramide
                  |
 a-D-Neup5Ac-(2-3)+
================end of record