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Whether a particular investigation is considered to be scientific depends on whether
Cystic Fibrosis
A genetic disease with an autosomal recessive inheritance pattern;
CFTR Protein
A protein that functions as a channel transporting chloride ions across cell membranes, mutations of which cause cystic fibrosis.
Genetic Disease
A disorder or condition caused by abnormalities in an individual's DNA, often inherited from one or both parents.
Amino Acid
An organic compound containing an amino group (—NH2) and a carboxyl group (—COOH); may be joined by peptide bonds to form a polypeptide chain.
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