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Analysis of extra- and intragenic marker haplotypes as part of molecular diagnosis of cystic fibrosis in patients from Serbia

Cystic fibrosis (CF) is the most common fatal autosomal recessive disease in Caucasians. Since characterization of F508del, the predominant mutation in different countries, more than 1500 mutations have been discovered in the CFTR gene, including a large number of polymorphisms. After molecular scre...

पूर्ण विवरण

में बचाया:
ग्रंथसूची विवरण
मुख्य लेखकों: Radivojević Danijela, Lalić Tanja, Đurišić Marina, Guć-Šćekić Marija, Minić P., Sovtić A.
स्वरूप: Artigo
भाषा:Inglês
प्रकाशित: University of Belgrade, University of Novi Sad 2008-01-01
श्रृंखला:Archives of Biological Sciences
विषय:
ऑनलाइन पहुंच:http://www.doiserbia.nb.rs/img/doi/0354-4664/2008/0354-46640801005R.pdf
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