19 min listen
Matching Drugs to Genetic Abnormalities to Precisely Treat Cystic Fibrosis
Matching Drugs to Genetic Abnormalities to Precisely Treat Cystic Fibrosis
ratings:
Length:
26 minutes
Released:
Dec 5, 2017
Format:
Podcast episode
Description
Cystic fibrosis is a common autosomal recessive disease. It is caused by any one of many discrete genetic abnormalities that affect chloride transport. Identification of specific genetic abnormalities enables clinicians to identify drugs that counteract the effects of the abnormal genes. In this podcast we review how genetic defects that cause cystic fibrosis are identified and how drugs that are likely to successfully treat the disease are matched to those genetic abnormalities. Related article
Released:
Dec 5, 2017
Format:
Podcast episode
Titles in the series (100)
Achalasia: The JAMA Clinical Review by JAMA Clinical Reviews