Cystic Fibrosis Detection of CFTR gene duplications/deletions by MLPA (including point mutation DF508)

GenoLife
Caja de Cystic Fibrosis Detection of CFTR gene duplications/deletions by MLPA (including point mutation DF508)

Delivery time

No especificado

Sample

No especificado

582,00€
Caja de Cystic Fibrosis Detection of CFTR gene duplications/deletions by MLPA (including point mutation DF508)

Cystic fibrosis is an inherited disorder that causes severe damage to the lungs, digestive system, and other organs in the body.

Cystic fibrosis affects the cells that produce mucus, sweat, and digestive juices. These secreted fluids are normally thin and slippery. But in people with cystic fibrosis, a defective gene causes the secretions to become sticky and thick. Instead of acting as lubricants, the secretions clog tubes, ducts, and passages, especially in the lungs and pancreas.

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