3d
alpha
autosomal
betahexosaminidase a
brain
cell
chemical
congenital
deficiency
demyelinating
demyelination
disease
disorder
enzyme
gangliosidosis
gene mutation
genetic
gm2
gm2 ganglioside
hexa
hexa gene
hexosaminidase a
human
illustration
infancy
infant
inherited
lamellar
lipid
lysosomal
lysosome
medical
membraneous
metabolic
molecular
myelin
neurology
neuron
neuropathy
ocular
pathology
polypeptide
recessive
science
sphingolipidosis
storage
storage disease
structure
taysachs
tsd
定額
Brain neurons in Tay-Sachs disease, 3D illustration showing swollen neurons with membraneous lamellar inclusions due to accumulation of gangliosides in lysosomes and demyelinationの素材 [FY310176958407]
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