k TaySachs disease, illustration TaySachs disease, illustration. A genetic disorder that progressively destroys brain neurons. It is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A. Taysachs is most commonly seen in infants, manifesting in muscle weakness and decreased motor function, vision and hearing loss, and intellectual disability., by KATERYNA KONSCIENCE PHOTO LIBRARY Stock Photo - Afloimages
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Tay Sachs disease, illustration Tay Sachs disease, illustration. A genetic disorder that progressively destroys brain neurons. It is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A. Tay sachs is most commonly seen in infants, manifesting in muscle weakness and decreased motor function, vision and hearing loss, and intellectual disability., by KATERYNA KON SCIENCE PHOTO LIBRARY
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Tay-Sachs disease, illustration

Tay-Sachs disease, illustration. A genetic disorder that progressively destroys brain neurons. It is caused by a mutation in the HEXA gene of chromosome 15 leading to deficiency of hexosaminidase A. Tay-sachs is most commonly seen in infants, manifesting in muscle weakness and decreased motor function, vision and hearing loss, and intellectual disability., by KATERYNA KON/SCIENCE PHOTO LIBRARY

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179833488

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0.3 MB
724 x 483 px
6.1 x 4.1 cm
$ 100.00
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3.3 MB
2290 x 1527 px
19.4 x 12.9 cm
$ 180.00
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21.3 MB
5787 x 3858 px
49 x 32.7 cm
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