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The scientists identify the DNA sequence of someone with the disease and then compare it to a person without the disease. By doing this they can recognize which gene is abnormal and causes the disease. This entire process is called the "Human Genome Project" and is being done in more than 200 laboratories, with more and more labs joining each year. Most of these labs are located in France and the United States. The project started in 1990 and was predicted to take 15 years and cost $3 billion. It costs the United States about $200 million per year. The $200 million per year has only covered about 60% of the annual need...
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