A novel missense mutation, R1283S, of the cystic fibrosis transmembrane conductance regulator gene in a 47-year-old African-American patient

Autor: Lynn Wang, Y., Chen, Ke-Lian, Joshi, Indira, Kotloff, Robert M., Leonard, Debra G.B., Wilson, Robert B.
Zdroj: Molecular Diagnosis; January 1997, Vol. 2 Issue: 3 p205-208, 4p
Abstrakt: More than 600 mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene have been described; however, at least 50% of the disease-associated mutations in the African-American population remain unknown. Reported here is a novel missense mutation, R1283S, in a 47-year-old African-American patient with mild cystic fibrosis.
Databáze: Supplemental Index