3d
alpha
autosomal
betahexosaminidase a
brain
cell
chemical
congenital
deficiency
demyelination
disease
disorder
dna
enzyme
fabry
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
molecule
neurology
neuron
niemannpick
ocular
pathology
polypeptide
recessive
sphingolipidosis
storage
storage disease
structure
taysachs
tsd
定額
Brain neurons in lysosomal storage diseases, Tay-Sachs, Niemann-Pick, Fabry and other. 3D illustration showing swollen neurons with lamellar inclusions due to accumulation of gangliosides in lysosomesの素材 [FY310177151674]
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