Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens
LetterAçık Erişim
Anahtar Kelimeler
Cystic FibrosisFemaleHumansInfertility, MaleMaleMale Urogenital DiseasesPregnancycystic fibrosis transmembrane conductance regulatoradultaplasiaazoospermiaclinical articleethnic groupgene mutationgene sequencegenotypehumanlettermale genital tract malformationnucleotide sequenceTurkey (republic)vas deferens
RDL Kalıcı Bağlantı (PID)
https://rdlopen.rawdatalibrary.net/r/ebyu/15918Resmi atıflarda kullanılan kalıcı adresTam Kayıt
| Alan | Değer | Dil |
|---|---|---|
| dc.contributor.author | Akin, Y. | |
| dc.contributor.author | Demir, D. | |
| dc.contributor.author | Görgişen, G. | |
| dc.contributor.author | Lüleci, G. | |
| dc.contributor.author | Alper, Ö. M. | |
| dc.contributor.author | Watanabe, C.S. | |
| dc.contributor.author | Sahiner, I.F. | |
| dc.contributor.author | Usta, M.F. | |
| dc.date.accessioned | 2026-10-18T20:30:45.981349138Z | |
| dc.date.available | 2026-10-18T20:30:45.981349138Z | |
| dc.date.issued | 2014 | |
| dc.identifier.doi | 10.1111/and.12053 | |
| dc.identifier.eissn | 1439-0272 | |
| dc.identifier.endpage | 199 | |
| dc.identifier.issn | 0303-4569 | |
| dc.identifier.issue | 2 | |
| dc.identifier.pmid | 23240968 | |
| dc.identifier.scopus | 2-s2.0-84893436207 | |
| dc.identifier.startpage | 198 | |
| dc.identifier.uri | https://rdlopen.rawdatalibrary.net/r/ebyu/15918 | |
| dc.identifier.volume | 46 | |
| dc.identifier.wos | WOS:000331275800019 | |
| dc.language.iso | en | |
| dc.publisher | Blackwell Publishing Ltd | |
| dc.relation.ispartof | Andrologia | |
| dc.rights | info:eu-repo/semantics/openAccess | |
| dc.subject | Cystic Fibrosis | |
| dc.subject | Female | |
| dc.subject | Humans | |
| dc.subject | Infertility, Male | |
| dc.subject | Male | |
| dc.subject | Male Urogenital Diseases | |
| dc.subject | Pregnancy | |
| dc.subject | cystic fibrosis transmembrane conductance regulator | |
| dc.subject | adult | |
| dc.subject | aplasia | |
| dc.subject | azoospermia | |
| dc.subject | clinical article | |
| dc.subject | ethnic group | |
| dc.subject | gene mutation | |
| dc.subject | gene sequence | |
| dc.subject | genotype | |
| dc.subject | human | |
| dc.subject | letter | |
| dc.subject | male genital tract malformation | |
| dc.subject | nucleotide sequence | |
| dc.subject | Turkey (republic) | |
| dc.subject | vas deferens | |
| dc.title | Novel and rare CFTR gene mutations in Turkish patients with congenital aplasia of vas deferens | |
| dc.type | Letter | |
| dspace.entity.type | Publication | |
| rdl.citation.scopus | 0 | |
| rdl.citation.wos | 0 | |
| rdl.department | Department of Urology, Erzincan University School of Medicine, Erzincan, Turkey. yigitakin@yahoo.com. | |
| rdl.source.index | SCOPUS | |
| rdl.source.index | WOS | |
| rdl.source.index | PUBMED | |
| rdl.wos.index | Science Citation Index Expanded (SCI-EXPANDED) |
