Interested in what the more medically/genetically minded on here think.
I read somewhere that Prader-Willi affects approximately 1/10,000 people and that people suffering from it are missing a portion of chromosome 15, from the paternal side of the family. When a portion of the same chromosome is missing from the Maternal side, the person may suffer from Angelman Syndrome.
Does it stand to reason that if we get positive results tomorrow, we can infer that we will also get positive results in a Prader-Willi trial or is it not that simple?
Interested in what the more medically/genetically minded on here...
Add NEU (ASX) to my watchlist
 (20min delay)
|
|||||
|
Last
$14.80 |
Change
-0.830(5.31%) |
Mkt cap ! $1.924B | |||
| Open | High | Low | Value | Volume |
| $15.65 | $15.72 | $14.76 | $11.61M | 772.4K |
Buyers (Bids)
| No. | Vol. | Price($) |
|---|---|---|
| 1 | 1392 | $14.80 |
Sellers (Offers)
| Price($) | Vol. | No. |
|---|---|---|
| $14.90 | 1553 | 2 |
View Market Depth
| Last trade - 16.10pm 19/11/2024 (20 minute delay) ? |
| NEU (ASX) Chart |