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  • Glicoesfingolipídeo que se acumula devido a uma deficiência de hexosaminidase A ou B (BETA-N-ACETIL-HEXOSAMINIDASE), ou da proteína ativadora de GM2, resultando em GANGLIOSIDOSES, transtornos metabólicos hereditários que incluem a DOENÇA DE TAY-SACHS e DOENÇA DE SANDHOFF.
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Anon_1   (more)
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