Zobrazeno 1 - 2
of 2
pro vyhledávání: '"Esma Bentli"'
Autor:
Semih Yilmaz, Esma Bentli, Berkay Saraymen, Bulent Zulfikar, Başak Koç Şenol, Davut Albayrak, Canan Albayrak, Emine Zengin, Aysun Çetin, Bülent Eser, Nazan Sarper, Mustafa Cetin, Sabahattin Muhtaroglu, Mustafa Yavuz Köker
Publikováno v:
Turkish Journal of Medical Sciences
SCI-Expanded Q4 WOS:000691664800006 PMID: 33957723 Background/aim: Glanzmann thrombasthenia (GT) is a rare autosomal recessively inherited bleeding disorder characterized by the quantitative (type 1 and type 2) or qualitative (type 3) deficiency in p
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::77e9115f8080bc407536815d0f49009e
https://pubmed.ncbi.nlm.nih.gov/33957723
https://pubmed.ncbi.nlm.nih.gov/33957723
Autor:
Zeynep Akidagi, Sevgi Bilgic Eltan, Bengu Akcam, Ercan Nain, Gamze Akgun, Elif Karakoc-Aydiner, Ahmet Ozen, Ismail Ogulur, Derya Ufuk Altintas, Safa Baris, Hatice Ezgi Baris, Dilek Karagöz, Dilek Baser, Esma Bentli, Berkay Saraymen, Sezin Aydemir, Gozde Yesil, Nurhan Kasap, Mustafa Yavuz Köker, Ayca Kiykim, Yildiz Camcioglu
Background Chronic granulomatous disease (CGD) is characterized by defective microbial killing due to mutations affecting subunits of the nicotinamide adenine dinucleotide phosphate (NADPH) oxidase complex. Definitive genetic identification of diseas
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4a684971750209d9b6643a2c186aff5d
https://aperta.ulakbim.gov.tr/record/11851
https://aperta.ulakbim.gov.tr/record/11851
