An Egyptian infant with cystic fibrosis mutation N1303K
Joint Authors
Wahhab A. A.
Marafyyah, M. M.
Janahi, I. A.
Source
Issue
Vol. 13, Issue 1 (30 Jun. 2004), pp.40-41, 2 p.
Publisher
Publication Date
2004-06-30
Country of Publication
Qatar
No. of Pages
2
Main Subjects
Topics
Abstract EN
An Egyptian infan( with the common CFTR mutation V1303Kin exon 21 developed alkalosis, electrolyte distur-hance and pancreas insufficiency, ! he need is emphasized to consider the possibility of cystic fibrosis (CF) in the Arab world.
The frequency of N1303K mutation in the Middle East audits distribution are both reviewed.
American Psychological Association (APA)
Wahhab A. A.& Janahi, I. A.& Marafyyah, M. M.. 2004. An Egyptian infant with cystic fibrosis mutation N1303K. Qatar Medical Journal،Vol. 13, no. 1, pp.40-41.
https://search.emarefa.net/detail/BIM-572522
Modern Language Association (MLA)
Wahhab A. A.…[et al.]. An Egyptian infant with cystic fibrosis mutation N1303K. Qatar Medical Journal Vol. 13, no. 1 (Jun. 2004), pp.40-41.
https://search.emarefa.net/detail/BIM-572522
American Medical Association (AMA)
Wahhab A. A.& Janahi, I. A.& Marafyyah, M. M.. An Egyptian infant with cystic fibrosis mutation N1303K. Qatar Medical Journal. 2004. Vol. 13, no. 1, pp.40-41.
https://search.emarefa.net/detail/BIM-572522
Data Type
Journal Articles
Language
English
Notes
Includes bibliographical references : p. 41
Record ID
BIM-572522
