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CF Genetics: The Basics | Cystic Fibrosis Foundation
https://www.cff.org/intro-cf/cf-genetics-basics
WEBSummary. Cystic fibrosis is caused by mutations in the gene that produces the cystic fibrosis transmembrane conductance regulator (CFTR) protein. In people with CF, mutations in the CFTR gene can disrupt the normal production or functioning of the CFTR protein found in the cells of the lungs and other parts of the body.
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Cystic fibrosis - Symptoms and causes - Mayo Clinic
https://www.mayoclinic.org/diseases-conditions/cystic-fibrosis/symptoms-causes/syc-20353700
WEBNov 23, 2021 · Simply put, cystic fibrosis is a gene defect. A defect to this gene changes how a salt moves in and out of cells, resulting in thick, sticky mucus in the respiratory, digestive and reproductive systems. It's an inherited condition. A child needs to inherit one copy of the mutated gene from each parent to develop cystic fibrosis.
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Cystic fibrosis - Wikipedia, the free encyclopedia
https://en.wikipedia.org/wiki/Cystic_fibrosis
WEBCystic fibrosis (also known as CF or mucoviscidosis) is an autosomal recessive genetic disorder affecting most critically the lungs, and also the pancreas, liver, and intestine.
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The genetics and genomics of cystic fibrosis - PMC
https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8008819/
WEB1. Background. Since the discovery of Cystic Fibrosis Transmembrane Conductance Regulator ( CFTR ) gene in 1989 [ 1 – 3 ], the CF Mutation Database (CFMD available at http://www.genet.sickkids.on.ca/cftr/) has been a valuable repository for DNA variants. As of 2019, 2065 variants in the CFTR gene have been inventoried by the CFMD.
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About Cystic Fibrosis - National Human Genome Research Institute
https://www.genome.gov/Genetic-Disorders/Cystic-Fibrosis
WEBDec 27, 2013 · About Cystic Fibrosis. Cystic fibrosis (CF) is the most common, fatal genetic disease in the United States. About 30,000 people in the United States have the disease. CF causes the body to produce thick, sticky mucus that clogs the lungs, leads to infection, and blocks the pancreas, which stops digestive enzymes from reaching the intestine ...
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Cystic fibrosis: MedlinePlus Genetics
https://medlineplus.gov/genetics/condition/cystic-fibrosis/
WEBDescription. Cystic fibrosis is an inherited disease characterized by the buildup of thick, sticky mucus that can damage many of the body's organs. The disorder's most common signs and symptoms include progressive damage to the respiratory system and chronic digestive system problems.
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Cystic Fibrosis | Johns Hopkins Medicine
https://www.hopkinsmedicine.org/health/conditions-and-diseases/cystic-fibrosis
WEBCF makes mucus thicker. Symptoms start in childhood. On average, people with CF live into their mid to late 30s. But new treatments are increasing life expectancy. CF affects several organ systems, including: Respiratory system. Digestive system. Reproductive system. Some people carry the CF gene without being affected by the disease.
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About Cystic Fibrosis | Cystic Fibrosis Foundation
https://www.cff.org/intro-cf/about-cystic-fibrosis
WEBCystic fibrosis is a progressive, genetic disease that affects the lungs, pancreas, and other organs. There are close to 40,000 children and adults living with cystic fibrosis in the United States (and an estimated 105,000 people have been diagnosed with CF across 94 countries), and CF can affect people of every racial and ethnic group.
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Genetics and CF | The Cystic Fibrosis Center at Stanford
https://med.stanford.edu/cfcenter/education/english/Genetics.html
WEBCystic fibrosis is a genetic disorder caused by inheriting a pair of genes that are mutated or not working properly. The Cystic Fibrosis Gene. Everyone inherits two copies of the CFTR (cystic fibrosis transmembrane conductance regulator) gene. However, some of the inherited copies are mutations.
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Role of Genetics in CF | Cystic Fibrosis Foundation
https://www.cff.org/intro-cf/role-genetics-cf
WEBCF Genetics: The Basics. Every person has two copies of the cystic fibrosis transmembrane conductance regulator (CFTR) gene. A person must inherit two copies of the CFTR gene that contain mutations — one copy from each parent — to have cystic fibrosis. 6 min read. ARTICLE. Basics of the CFTR Protein.
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