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Q57177269-E36E9AFC-C604-44E2-BB0C-CD2C100DB8DF
Q57177269-E36E9AFC-C604-44E2-BB0C-CD2C100DB8DF
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http://www.wikidata.org/entity/statement/Q57177269-E36E9AFC-C604-44E2-BB0C-CD2C100DB8DF
Phenotypic Characterization of the c.1679+1643G>T (1811+1643G>T) Mutation in Hispanic Cystic Fibrosis Patients
P2860
Q57177269-E36E9AFC-C604-44E2-BB0C-CD2C100DB8DF
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Statement
http://www.wikidata.org/entity/statement/Q57177269-E36E9AFC-C604-44E2-BB0C-CD2C100DB8DF
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wasDerivedFrom
2ddee0af9b6c2455796a9850bdce5c5c295eca6e
P2860
A novel donor splice site in intron 11 of the CFTR gene, created by mutation 1811+1.6kbA-->G, produces a new exon: high frequency in Spanish cystic fibrosis chromosomes and association with severe phenotype.