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ElenaFalcon
Guest
<P>DEAR ALL, my 7 month baby has been diagnosed with CF. Borderline sweat tests, pancreatic sufficient. The genetic testing revealed a single DF508 mutation, and the p.Phe10781le (or p.Phe1078lle - sorry, the spelling is not clear). The lab test indicated that this thing has NEVER been described before, it may be a missens mut and "likely to be clinically significant", which, in conjunction with the DF508 mutation, resulted in the diagnosis. I have NOT been able to find any information on this. </P>
<DIV>Can anyone point me in the direction of some resources for p.Phe10781le (or p.Phe1078lle)by itself, or in conjunction with single DF508?</DIV>
<DIV>Many thanks</DIV>
<DIV>Can anyone point me in the direction of some resources for p.Phe10781le (or p.Phe1078lle)by itself, or in conjunction with single DF508?</DIV>
<DIV>Many thanks</DIV>