Number of the records: 1
G(M2) gangliozid
SYS d005678 LBL 00000cz--a2200000n--4500 005 20250606213234.2 008 921119|||anznnbabn-----------|-a|a------ 040 $b slo $a DNLM $d BA006 $d BA006 $d BA006 065 $a D09.400.410.420.025.475.400 065 $a D10.390.470.025.475.400 065 $a D10.570.877.360.025.475.400 066 $a 01 $c 03 150 $a G(M2) gangliozid $x AA $x AD $x AE $x AG $x AI $x AN $x BI $x BL $x CF $x CH $x CL $x CS $x DF $x EC $x GE $x HI $x IM $x IP $x ME $x PD $x PH $x PK $x PO $x RE $x SD $x ST $x TO $x TU $x UR $2 slo 450 $w v $a GM2 Ganglioside $2 eng 450 $w v $a Tay-Sachs Disease Ganglioside $2 eng 450 $w v $a GM2 gangliozid $2 slo 450 $w v $a gangliozid Tayovej-Sachsovej choroby $2 slo 450 $w v $a gangliozid Tay-Sachsovej choroby $2 slo 550 $7 sllk_us_auth*d012497 $Y Sandhoff Disease $w p $a Sandhoffova choroba 550 $7 sllk_us_auth*d013661 $Y Tay-Sachs Disease $w p $a Tay-Sachsova choroba 665 $a 91(75); was see under GANGLIOSIDES 1975-90 $2 eng 665 $a Gangliosides (1974) $2 eng 680 9-
$i A glycosphingolipid that accumulates due to a deficiency of hexosaminidase A or B (BETA-N-ACETYLHEXOSAMINIDASES), or GM2 activator protein, resulting in GANGLIOSIDOSES, heredity metabolic disorders that include TAY-SACHS DISEASE and SANDHOFF DISEASE. $2 eng 750 -2
$a G(M2) Ganglioside $2 eng 980 $x M
Number of the records: 1