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Stock image Tay-Sachs disease, 3D illustration. A genetic disorder that progressively destroys brain neurons, is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A
Published:
Oct.12, 2021 09:05:24
Author:
katerynakon
Views:
343
Downloads:
2
File type:
image
/
jpg
File size:
24.4 MB
Orginal size:
14000
x
8436
px
Available sizes:
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(500 x 301)
M
(1000 x 603)
L
(2000 x 1205)
XL
(14000 x 8436)
EL0
(14000 x 8436)
Level:
silver
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Image topics:
Illustration
Storage
Child
3d
Eye
Disease
Baby
Infant
Mutation
Genetic
Brain
Diagram
Dna
Molecule
Neuron
Deficiency
Disorder
Jew
Neurology
Congenital
Metabolism
Retina
Gene
Enzyme
Hexa
Metabolic
Lipid
Recessive
Ashkenazi
Ophthalmoscope
Macula
Inherited
Lysosome
Autosomal
Polypeptide
Demyelination
Tsd
GM2
Gangliosidosis
Chromosome 15
Macrocephaly
Lysosomal
Sphingolipidosis
Tay Sachs
Ganglioside
Hexa Gene
Hexosaminidase A
Beta Hexosaminidase A
Gm2 Ganglioside
Cherry Red Spot
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