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Rectal Organoid Morphology Analysis (ROMA): A Diagnostic Assay in Cystic Fibrosis
Published on: June 10, 2022
Bayesian risk assessment for autosomal recessive diseases: fetal echogenic bowel with one or no detectable CFTR
S Ogino1, R B Wilson, W W Grody
1Department of Pathology, Brigham and Women's Hospital, Boston, Massachusetts 02115 USA. sogino@partners.org
Journal of Medical Genetics
|May 4, 2004
Abstract
No abstract available in PubMed .
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Cystic fibrosis (CF), an autosomal recessive disorder, significantly affects the function of exocrine glands. This genetically inherited disease is characterized by the production of thick and sticky mucus, which can severely affect various organs and systems in the body.
CF is primarily caused by a genetic mutation in a chromosome 7 gene coding for the cystic fibrosis transmembrane conductance regulator (CFTR) protein. The most common gene mutation leading to CF is the ΔF508 mutation, but...
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