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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.18, 2021 11:43:36
Author:
katerynakon
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20
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0
File type:
image
/
jpg
File size:
11.31 MB
Orginal size:
11483
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8436
px
Available sizes:
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(500 x 367)
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Level:
silver
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Image topics:
Illustration
Storage
3d
Eye
Disease
Infant
Mutation
Genetic
Brain
Diagram
Dna
Molecule
Neuron
Deficiency
Disorder
Jew
Neurology
Congenital
Metabolism
Retina
Gene
Enzyme
Hexa
Metabolic
Lipid
Recessive
Ashkenazi
Macula
Inherited
White Background
Lysosome
Autosomal
Polypeptide
Demyelination
Tsd
GM2
Gangliosidosis
Chromosome 15
Macrocephaly
Lysosomal
Sphingolipidosis
Gene Mutation
Tay Sachs
Ganglioside
Hexa Gene
Hexosaminidase A
Storage Disease
Beta Hexosaminidase A
Gm2 Ganglioside
Cherry Red Spot
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