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515346636
- Id: 515346636
- Media type: Photography
- Author: katerynakon
- Keywords:
illustration human storage medical structure cell disease chemical infant genetic brain dna molecule molecular neuron deficiency disorder ocular neurology infancy congenital pathology membraneous lamellar enzyme alpha hexa metabolic Lipid recessive inherited lysosome autosomal polypeptide demyelination tsd GM2 gangliosidosis Fabry lysosomal sphingolipidosis gene mutation tay sachs niemann pick hexa gene hexosaminidase a storage disease beta hexosaminidase a gm2 ganglioside
Categories
| Size | Width | Height | Mp |
|---|---|---|---|
| s | 500 px | 281 px | 0.5 |
| m | 1000 px | 563 px | 2 |
| l | 2000 px | 1125 px | 8 |
| xl | 7200 px | 4050 px | 15 |
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