CFTR gene and protein;
chloride channel;
cystic fibrosis;
genetic mutation;
D O I:
10.1016/j.actpha.2024.06.005
中图分类号:
R9 [药学];
学科分类号:
1007 ;
摘要:
Learn more about cystic fibrosis . Cystic fibrosis is a widespread disease worldwide, and the most common rare hereditary genetic disorder in Western populations. Many organs are affected in cystic fibrosis patients. Lesions are linked to dysfunction of an ion channel, the CFTR protein, whose synthesis can be altered by various types of mutation. Pharmacists must be able to inform patients and their families about this disease. (c) 2024 Elsevier Masson SAS. All reserved
机构:
Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA
Melese, M
Alemayehu, W
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机构:
Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA
Alemayehu, W
Gaynor, B
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机构:
Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA
Gaynor, B
Yi, E
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机构:
Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA
Yi, E
Whitcher, JP
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Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA
Whitcher, JP
Lietman, TM
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机构:
Univ Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USAUniv Calif San Francisco, Francis I Proctor Fdn, Dept Ophthalmol, San Francisco, CA 94143 USA