| 1. | Missense mutations in the 7TM region resulted in loss of signalling.
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| 2. | There are also 28 potential missense mutations in the human C3orf70.
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| 3. | Two missense mutations are the most common cause of the deficiency.
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| 4. | With this process, both nonsense and missense mutations are possible.
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| 5. | Many missense mutations of the LQT1 gene have been identified.
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| 6. | This dysfunction results from a missense mutation that effects the encoded TPI protein.
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| 7. | Not all missense mutations lead to appreciable protein changes.
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| 8. | Cancer associated missense mutations can lead to drastic destabilisation of the resulting protein.
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| 9. | Nonsense and missense mutations cause the most severe phenotypes.
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| 10. | Another POR missense mutation Y181D has also been identified.
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