mjl1717
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Hutchinson Gilford syndrome [Progeria] is caused by mutation in which gene
a) Lamin A
b) Lamin B
c) Lamin C
d) Lamin D
e)Lamin E
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| msyamp
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well i just read about it because of the farnesyl esterase inhibitor question. it is a defect in lamin A. its mutation causes nuclear envelop unstable and develops aging verf fast.
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| reet
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LAMIN A
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