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Science
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2 / 483 |
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Hopefully further studies and research of TSD will mean it will no longer be a fatal disease for infants. The end of TSD will bring hope to families wanting to have children but who are both carriers of the recessive gene.
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This rare hereditary disease is caused by a genetic mutation that leaves the body unable to produce an enzyme; a protein that speeds up the rate at which chemical reactions take place within the body. The enzyme is necessary for nerve cells to metabolise fat, (allow for chemical reactions to take place within the cell) ...
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